Canonical Allele Identifier: CA1328965644

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893239C= , CM000664.2:g.218893239C=	GRCh38
NC_000002.11:g.219757961C= , CM000664.1:g.219757961C=	GRCh37
NC_000002.10:g.219466205C=	NCBI36
NG_012179.1:g.17707C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1222C= MANE Select	ENSP00000258411.3:p.Arg408=
ENST00000258411.7:c.1222C=	ENSP00000258411.3:p.Arg408=
ENST00000489887.1:n.19C=
NM_025216.2:c.1222C=	NP_079492.2:p.Arg408=
XM_011511928.1:c.1171C=	XP_011510230.1:p.Arg391=
XM_011511929.1:c.1126C=	XP_011510231.1:p.Arg376=
XM_011511930.1:c.842C=	XP_011510232.1:p.Pro281=
XM_011511929.2:c.1126C=	XP_011510231.1:p.Arg376=
NM_025216.3:c.1222C= MANE Select	NP_079492.2:p.Arg408=