Gene
TCTA
T cell leukemia translocation altered
- HGNC 11692↗(opens in a new tab)
- Ensembl gene ENSG00000145022↗(opens in a new tab)
- NCBI Gene 6988↗(opens in a new tab)
Summary
- Cytogenetic location
- 3p21.31
- Coordinates
- Chromosome 3: 49,412,423–49,416,476 (GRCh38)
- Exons
- 3 exons across 4.1 kb
- Protein
- 103 amino acids
- MANE Select transcript
- ENST00000273590.4NM_022171.3
- Locus type
- gene with protein product
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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How TCTA is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 1.9 kb of the gene's 4.1 kb; 312 of those bases code for the protein.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
Cite this page
Dante Labs. (n.d.). TCTA gene: T cell leukemia translocation altered. Retrieved 16 October 2026, from https://dantelabs.com/genes/tcta
Dante Labs. TCTA gene: T cell leukemia translocation altered [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/tcta
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