Canonical Allele Identifier: CA1328965583

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893197T= , CM000664.2:g.218893197T=	GRCh38
NC_000002.11:g.219757919T= , CM000664.1:g.219757919T=	GRCh37
NC_000002.10:g.219466163T=	NCBI36
NG_012179.1:g.17665T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1180T= MANE Select	ENSP00000258411.3:p.Cys394=
ENST00000258411.7:c.1180T=	ENSP00000258411.3:p.Cys394=
NM_025216.2:c.1180T=	NP_079492.2:p.Cys394=
XM_011511928.1:c.1129T=	XP_011510230.1:p.Cys377=
XM_011511929.1:c.1084T=	XP_011510231.1:p.Cys362=
XM_011511930.1:c.800T=	XP_011510232.1:p.Leu267=
XM_011511929.2:c.1084T=	XP_011510231.1:p.Cys362=
NM_025216.3:c.1180T= MANE Select	NP_079492.2:p.Cys394=