Canonical Allele Identifier: CA1328965680

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893269T= , CM000664.2:g.218893269T=	GRCh38
NC_000002.11:g.219757991T= , CM000664.1:g.219757991T=	GRCh37
NC_000002.10:g.219466235T=	NCBI36
NG_012179.1:g.17737T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1252T= MANE Select	ENSP00000258411.3:p.Ter418=
ENST00000258411.7:c.1252T=	ENSP00000258411.3:p.Ter418=
ENST00000489887.1:n.47+2T=
NM_025216.2:c.1252T=	NP_079492.2:p.Ter418=
XM_011511928.1:c.1201T=	XP_011510230.1:p.Ter401=
XM_011511929.1:c.1156T=	XP_011510231.1:p.Ter386=
XM_011511930.1:c.872T=	XP_011510232.1:p.Val291=
XM_011511929.2:c.1156T=	XP_011510231.1:p.Ter386=
NM_025216.3:c.1252T= MANE Select	NP_079492.2:p.Ter418=