--- title: "ACTA1 C376F (c.1127G>T, rs1571892196) | Dante Labs" description: "ClinVar classifies ACTA1 C376F as Likely pathogenic (reviewed by expert panel). Where it sits in the genome, its predicted effect, and the Genome Test reports that look at it." url: "https://dantelabs.com/genes/acta1/variants/c376f" --- 1. [Genes](https://dantelabs.com/genes) 2. [ACTA1](https://dantelabs.com/genes/acta1) 3. ACTA1 C376F Variant # ACTA1 C376F NM_001100.4(ACTA1):c.1127G>T (p.Cys376Phe) Also known as - p.Cys376Phe - p.C376F - rs1571892196 * ClinVar classification Likely pathogenic * Review status 3 stars out of 4 reviewed by expert panel * Last evaluated 27 August 2024 * Expert panel ClinGen Congenital Myopathies Variant Curation Expert Panel, ClinGen Data current to ClinVar release 2026-10-12 · Dante Labs data release 2026.10.16-c6eea6bf Facts last changed 16 October 2026 ## Summary C376F is a missense variant in ACTA1: it changes a single amino acid in the protein the gene encodes. ClinVar classifies it as likely pathogenic for ACTA1-related myopathy (alpha-actinopathy) (reviewed by expert panel). ## ClinVar classifications | Condition | Classification | Review status | Submissions | Last evaluated | | -------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------------- | ----------------- | ----------------------------------------- | ------------ | -------------- | | [ACTA1-related myopathy (alpha-actinopathy)](https://dantelabs.com/conditions/congenital-myopathies) [ClinVar VCV000801630 (opens in a new tab)](https://www.ncbi.nlm.nih.gov/clinvar/variation/801630/) | Likely pathogenic | 3 stars out of 4 reviewed by expert panel | 1 submission | 27 August 2024 | Classifications as ClinVar records them in release 2026-10-12. ClinVar updates them as evidence is reviewed. ## Where it lies in ACTA1 C376F lies in exon 7 of the 7 in ACTA1's MANE Select transcript, NM_001100.4. [ACTA1 variants in exon 7 →](https://dantelabs.com/genes/acta1/variants?exon=7) [ACTA1's gene diagram →](https://dantelabs.com/genes/acta1#gene-structure) ## Molecular details | Gene | [ACTA1](https://dantelabs.com/genes/acta1) | | --------------------------- | ----------------------------------------------------------------------------------------------------------------------------------------------------- | | Transcript | NM_001100.4 MANE Select | | Coding DNA change (HGVS c.) | c.1127G>T | | Protein change (HGVS p.) | p.Cys376Phe p.C376F | | Predicted consequence | Missense [missense_variant (opens in a new tab)](https://purl.obolibrary.org/obo/SO_0001583) | | Predicted impact | Moderate | | Position (GRCh38) | chr1:229431506 C>A | | Position (GRCh37) | chr1:229567253 C>A | | dbSNP ID | [rs1571892196 (opens in a new tab)](https://www.ncbi.nlm.nih.gov/snp/rs1571892196) | | ClinVar Variation ID | [VCV000801630 (opens in a new tab)](https://www.ncbi.nlm.nih.gov/clinvar/variation/801630/) | | ClinVar Allele ID | 789940 | | ClinGen Allele Registry ID | [CA345144073 (opens in a new tab)](https://reg.clinicalgenome.org/redmine/projects/registry/genboree_registry/by_canonicalid?canonicalid=CA345144073) | | ClinVar name | NM_001100.4(ACTA1):c.1127G>T (p.Cys376Phe) | ## ACTA1 C376F in other databases - [ClinVar VCV000801630 (opens in a new tab)](https://www.ncbi.nlm.nih.gov/clinvar/variation/801630/) - [dbSNP rs1571892196 (opens in a new tab)](https://www.ncbi.nlm.nih.gov/snp/rs1571892196) - [ClinGen Allele Registry CA345144073 (opens in a new tab)](https://reg.clinicalgenome.org/redmine/projects/registry/genboree_registry/by_canonicalid?canonicalid=CA345144073) - [gnomAD 1-229431506-C-A (opens in a new tab)](https://gnomad.broadinstitute.org/variant/1-229431506-C-A?dataset=gnomad_r4) - [Ensembl rs1571892196 (opens in a new tab)](https://www.ensembl.org/Homo_sapiens/Variation/Explore?v=rs1571892196) ## Reports that look at this variant (1) These Genome Test condition reports include C376F among the variants they look at. | Report | Conditions | Inheritance | | ------------------------------------------------------------------------------- | ------------------------------------------ | ----------- | | [Congenital Myopathies](https://dantelabs.com/conditions/congenital-myopathies) | ACTA1-related myopathy (alpha-actinopathy) | | ## Other variants in ACTA1 - [c.617-5C>A Likely pathogenic 3 stars out of 4](https://dantelabs.com/genes/acta1/variants/c-617-5c-a) - [c.687G>C Pathogenic 3 stars out of 4](https://dantelabs.com/genes/acta1/variants/c-687g-c) - [c.990+1G>T Pathogenic 3 stars out of 4](https://dantelabs.com/genes/acta1/variants/c-990plus1g-t) - [C376S Pathogenic 3 stars out of 4](https://dantelabs.com/genes/acta1/variants/c376s) - [D13E Likely pathogenic 3 stars out of 4](https://dantelabs.com/genes/acta1/variants/d13e) - [D13N Likely pathogenic 3 stars out of 4](https://dantelabs.com/genes/acta1/variants/d13n) - [D58N Likely pathogenic 3 stars out of 4](https://dantelabs.com/genes/acta1/variants/d58n) - [D181Tfs\*11 Pathogenic 3 stars out of 4](https://dantelabs.com/genes/acta1/variants/d181tfs11) - [D290H Pathogenic 3 stars out of 4](https://dantelabs.com/genes/acta1/variants/d290h) - [E59K Likely pathogenic 3 stars out of 4](https://dantelabs.com/genes/acta1/variants/e59k) [All ACTA1 variants](https://dantelabs.com/genes/acta1/variants) ## Limitations This page describes publicly available information about a genetic variant. It is not a diagnosis, and it says nothing about whether you or anyone else carries this variant. Classifications come from ClinVar and change as new evidence is reviewed. A classification here may differ from the one in ClinVar today, or from the one a laboratory reports. Whole genome sequencing with short reads can miss or miscall some variants, particularly in repeated or highly similar stretches of DNA and in large insertions, deletions or rearrangements. If you have questions about a variant in your own results or in your family, talk to a genetic counsellor or your doctor. ## Sources & credits - Classifications from ClinVar (release 2026-10-12), National Center for Biotechnology Information. - Condition terms from the Mondo Disease Ontology (release 2026-10-06), used under CC BY 4.0. - Gene symbols and names from the HUGO Gene Nomenclature Committee (release 2026-10-16). - Allele identifiers from the ClinGen Allele Registry (release 2026-10-16-c4908f54). - Reference SNP identifiers from dbSNP (release b157), National Center for Biotechnology Information. - Gene–disease links from the Gene Curation Coalition, GenCC (release 2026-10-16). - Difficult regions from the Genome in a Bottle Consortium (release v3.6). - Transcripts from MANE (release v1.5), NCBI and EMBL-EBI. - Predicted consequences from mehari (release 0.11.0), with transcript models from cdot. - Built from Dante Labs data release 2026.10.16-c6eea6bf of 16 October 2026. ## Cite this page APA > Dante Labs. (16 October 2026). ACTA1 C376F (c.1127G>T, rs1571892196) (Version 2026.10.16-c6eea6bf). Retrieved 16 October 2026, from https\://dantelabs.com/genes/acta1/variants/c376f Vancouver > Dante Labs. ACTA1 C376F (c.1127G>T, rs1571892196) \[Internet]. Version 2026.10.16-c6eea6bf. 16 October 2026 \[cited 16 October 2026]. Available from: https\://dantelabs.com/genes/acta1/variants/c376f Download citation [RIS](https://dantelabs.com/genes/acta1/variants/c376f/cite.ris) [BibTeX](https://dantelabs.com/genes/acta1/variants/c376f/cite.bib) [CSL-JSON](https://dantelabs.com/genes/acta1/variants/c376f/cite.json) ## Read your whole genome From $449 Free shipping · Results in 6–8 weeks [Explore the Genome Test](https://dantelabs.com/whole-genome-sequencing)