Canonical Allele Identifier: CA359262260

Gene: MYO10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.16671498T>A , CM000667.2:g.16671498T>A	GRCh38
NC_000005.9:g.16671607T>A , CM000667.1:g.16671607T>A	GRCh37
NC_000005.8:g.16724607T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513610.6:c.5354A>T MANE Select	ENSP00000421280.1:p.Tyr1785Phe
ENST00000274203.13:c.5387A>T	ENSP00000274203.10:p.Tyr1796Phe
ENST00000505695.5:c.3371A>T	ENSP00000421170.1:p.Tyr1124Phe
ENST00000513610.5:c.5354A>T	ENSP00000421280.1:p.Tyr1785Phe
ENST00000515803.5:c.3371A>T	ENSP00000425051.1:p.Tyr1124Phe
NM_012334.2:c.5354A>T	NP_036466.2:p.Tyr1785Phe
XM_005248306.3:c.3428A>T	XP_005248363.1:p.Tyr1143Phe
XM_005248307.1:c.3425A>T	XP_005248364.1:p.Tyr1142Phe
XM_006714475.1:c.5285A>T	XP_006714538.1:p.Tyr1762Phe
XM_011514046.1:c.3425A>T	XP_011512348.1:p.Tyr1142Phe
XM_005248306.4:c.3428A>T	XP_005248363.1:p.Tyr1143Phe
XM_005248307.2:c.3425A>T	XP_005248364.1:p.Tyr1142Phe
XM_006714475.3:c.5285A>T	XP_006714538.1:p.Tyr1762Phe
XM_011514046.2:c.3425A>T	XP_011512348.1:p.Tyr1142Phe
NM_012334.3:c.5354A>T MANE Select	NP_036466.2:p.Tyr1785Phe