Canonical Allele Identifier: CA3210577

Gene: MYO10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.16666723C>T , CM000667.2:g.16666723C>T	GRCh38
NC_000005.9:g.16666832C>T , CM000667.1:g.16666832C>T	GRCh37
NC_000005.8:g.16719832C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513610.6:c.6146G>A MANE Select	ENSP00000421280.1:p.Arg2049His
ENST00000274203.13:c.6179G>A	ENSP00000274203.10:p.Arg2060His
ENST00000505695.5:c.4163G>A	ENSP00000421170.1:p.Arg1388His
ENST00000513610.5:c.6146G>A	ENSP00000421280.1:p.Arg2049His
ENST00000515803.5:c.4163G>A	ENSP00000425051.1:p.Arg1388His
NM_012334.2:c.6146G>A	NP_036466.2:p.Arg2049His
XM_005248306.3:c.4220G>A	XP_005248363.1:p.Arg1407His
XM_005248307.1:c.4217G>A	XP_005248364.1:p.Arg1406His
XM_006714475.1:c.6077G>A	XP_006714538.1:p.Arg2026His
XM_011514046.1:c.4217G>A	XP_011512348.1:p.Arg1406His
XM_005248306.4:c.4220G>A	XP_005248363.1:p.Arg1407His
XM_005248307.2:c.4217G>A	XP_005248364.1:p.Arg1406His
XM_006714475.3:c.6077G>A	XP_006714538.1:p.Arg2026His
XM_011514046.2:c.4217G>A	XP_011512348.1:p.Arg1406His
NM_012334.3:c.6146G>A MANE Select	NP_036466.2:p.Arg2049His