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Gene

MYH10

myosin heavy chain 10

Summary

Cytogenetic location
17p13.1
Coordinates
Chromosome 17: 8,474,224–8,630,725 (GRCh38)
Exons
43 exons across 156.5 kb
Protein
2,007 amino acids
Also known as
NMMHCB
MANE Select transcript
ENST00000360416.8NM_001256012.3
Locus type
gene with protein product

Reference genomeGRCh38

Positions on gene and variant pages follow this choice, in this browser.

Curated reports relevant to this gene

No Genome Test report reads MYH10 yet. The test sequences your whole genome, so your data includes it all the same.

How MYH10 is laid out

  • Coding sequence
  • Untranslated region
  • Intron
  • Direction of transcription
  • Known disease-causing sites
  • Stretches short reads find hard
Chromosome 17, with a bracket where MYH10 sits. MYH10 and 26 genes near it on chromosome 17, from 8,052,475 to 9,052,474.Chromosome 1717p13.1p13.3p13.2p13.1p12p11.2p11.1q11.1q11.2q12q21.1q21.2q21.31q21.32q21.33q22q23.1q23.2q23.3q24.1q24.2q24.3q25.1q25.2q25.38.2 Mb8.4 Mb8.6 Mb8.8 Mb9 MbALOX12B: 8,068,594–8,087,716, reverse strandALOX12BALOXE3: 8,095,900–8,119,047, reverse strandALOXE3HES7: 8,120,592–8,124,114, reverse strandHES7PER1: 8,140,467–8,156,506, reverse strand: 8,150,816–8,162,975, reverse strandVAMP2: 8,159,149–8,163,584, reverse strandVAMP2TMEM107: 8,172,440–8,176,408, reverse strandTMEM107BORCS6: 8,188,345–8,190,180, reverse strandBORCS6AURKB: 8,204,335–8,210,638, reverse strandAURKBCTC1: 8,224,815–8,248,075, reverse strandCTC1PFAS: 8,247,618–8,271,150, forward strandPFASSLC25A35: 8,287,762–8,295,410, reverse strandSLC25A35RANGRF: 8,288,631–8,290,092, forward strandRANGRFARHGEF15: 8,310,222–8,323,203, forward strandARHGEF15ODF4: 8,339,840–8,346,048, forward strandKRABD2: 8,356,902–8,376,738, reverse strandKRABD2: 8,368,638–8,383,187, reverse strandRPL26: 8,377,500–8,384,062, reverse strandRPL26RNF222: 8,390,702–8,397,827, reverse strandRNF222NDEL1: 8,408,528–8,501,107, forward strandNDEL1MYH10: 8,474,224–8,630,725, reverse strandMYH10CCDC42: 8,729,930–8,745,970, reverse strandCCDC42SPDYE4: 8,747,524–8,758,559, reverse strandSPDYE4MFSD6L: 8,797,110–8,799,365, reverse strandMFSD6LPIK3R6: 8,802,722–8,867,696, reverse strandPIK3R6PIK3R5: 8,878,911–8,966,008, reverse strandPIK3R5NTN1: 9,003,080–9,244,000, forward strandNTN1Diagram of MYH10: 43 exons on the reverse strand of chromosome 17Exon 42: 1 known disease-causing siteExon 39: 1 known disease-causing siteExon 43: 8,474,224–8,475,948, 1,725 basesExon 42: 8,476,876–8,477,048, 173 basesExon 41: 8,478,338–8,478,446, 109 basesExon 40: 8,480,110–8,480,318, 209 basesExon 39: 8,480,402–8,480,525, 124 basesExon 38: 8,481,322–8,481,410, 89 basesExon 37: 8,484,138–8,484,266, 129 basesExon 36: 8,487,433–8,487,594, 162 basesExon 35: 8,490,340–8,490,552, 213 basesExon 34: 8,492,297–8,492,509, 213 basesExon 33: 8,492,776–8,493,024, 249 basesExon 32: 8,493,733–8,493,885, 153 basesExon 31: 8,495,137–8,495,241, 105 basesExon 30: 8,499,270–8,499,476, 207 basesExon 29: 8,500,826–8,500,970, 145 basesExon 28: 8,504,694–8,504,906, 213 basesExon 27: 8,506,318–8,506,489, 172 basesExon 26: 8,508,554–8,508,677, 124 basesExon 25: 8,509,812–8,509,949, 138 basesExon 24: 8,512,451–8,512,657, 207 basesExon 23: 8,513,538–8,513,669, 132 basesExon 22: 8,513,786–8,513,894, 109 basesExon 21: 8,518,631–8,518,791, 161 basesExon 20: 8,518,881–8,518,950, 70 basesExon 19: 8,520,878–8,520,999, 122 basesExon 18: 8,521,092–8,521,285, 194 basesExon 17: 8,530,623–8,530,685, 63 basesExon 16: 8,535,387–8,535,501, 115 basesExon 15: 8,535,758–8,535,931, 174 basesExon 14: 8,542,107–8,542,280, 174 basesExon 13: 8,545,448–8,545,600, 153 basesExon 12: 8,546,544–8,546,662, 119 basesExon 11: 8,548,313–8,548,408, 96 basesExon 10: 8,548,644–8,548,787, 144 basesExon 9: 8,552,046–8,552,144, 99 basesExon 8: 8,553,955–8,554,018, 64 basesExon 7: 8,569,720–8,569,812, 93 basesExon 6: 8,576,643–8,576,672, 30 basesExon 5: 8,577,236–8,577,338, 103 basesExon 4: 8,589,081–8,589,108, 28 basesExon 3: 8,604,826–8,604,982, 157 basesExon 2: 8,622,902–8,623,277, 376 basesExon 1: 8,630,654–8,630,725, 72 bases4340353025201510515′3′

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 7.7 kb of the gene's 156.5 kb; 6,024 of those bases code for the protein.

How a genome test reads MYH10

3

positions in MYH10 where ClinVar classes a change as pathogenic or likely pathogenic

None of them falls in a region short reads find hard.

A whole genome covers all 156.5 kb of MYH10, introns included, not only the 7.7 kb of exons.

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.
  • ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
  • Data release 2026.10.16-c6eea6bf.

Cite this page

APA

Dante Labs. (n.d.). MYH10 gene: myosin heavy chain 10. Retrieved 16 October 2026, from https://dantelabs.com/genes/myh10

Vancouver

Dante Labs. MYH10 gene: myosin heavy chain 10 [Internet]. [cited 16 October 2026]. Available from: https://dantelabs.com/genes/myh10

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