Canonical Allele Identifier: CA1328965667

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893260G= , CM000664.2:g.218893260G=	GRCh38
NC_000002.11:g.219757982G= , CM000664.1:g.219757982G=	GRCh37
NC_000002.10:g.219466226G=	NCBI36
NG_012179.1:g.17728G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1243G= MANE Select	ENSP00000258411.3:p.Val415=
ENST00000258411.7:c.1243G=	ENSP00000258411.3:p.Val415=
ENST00000489887.1:n.40G=
NM_025216.2:c.1243G=	NP_079492.2:p.Val415=
XM_011511928.1:c.1192G=	XP_011510230.1:p.Val398=
XM_011511929.1:c.1147G=	XP_011510231.1:p.Val383=
XM_011511930.1:c.863G=	XP_011510232.1:p.Arg288=
XM_011511929.2:c.1147G=	XP_011510231.1:p.Val383=
NM_025216.3:c.1243G= MANE Select	NP_079492.2:p.Val415=