Canonical Allele Identifier: CA3210731

Gene: MYO10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.16670711G>A , CM000667.2:g.16670711G>A	GRCh38
NC_000005.9:g.16670820G>A , CM000667.1:g.16670820G>A	GRCh37
NC_000005.8:g.16723820G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513610.6:c.5698C>T MANE Select	ENSP00000421280.1:p.Arg1900Trp
ENST00000274203.13:c.5731C>T	ENSP00000274203.10:p.Arg1911Trp
ENST00000505695.5:c.3715C>T	ENSP00000421170.1:p.Arg1239Trp
ENST00000513610.5:c.5698C>T	ENSP00000421280.1:p.Arg1900Trp
ENST00000515803.5:c.3715C>T	ENSP00000425051.1:p.Arg1239Trp
NM_012334.2:c.5698C>T	NP_036466.2:p.Arg1900Trp
XM_005248306.3:c.3772C>T	XP_005248363.1:p.Arg1258Trp
XM_005248307.1:c.3769C>T	XP_005248364.1:p.Arg1257Trp
XM_006714475.1:c.5629C>T	XP_006714538.1:p.Arg1877Trp
XM_011514046.1:c.3769C>T	XP_011512348.1:p.Arg1257Trp
XM_005248306.4:c.3772C>T	XP_005248363.1:p.Arg1258Trp
XM_005248307.2:c.3769C>T	XP_005248364.1:p.Arg1257Trp
XM_006714475.3:c.5629C>T	XP_006714538.1:p.Arg1877Trp
XM_011514046.2:c.3769C>T	XP_011512348.1:p.Arg1257Trp
NM_012334.3:c.5698C>T MANE Select	NP_036466.2:p.Arg1900Trp