Canonical Allele Identifier: CA1328965574

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893193C= , CM000664.2:g.218893193C=	GRCh38
NC_000002.11:g.219757915C= , CM000664.1:g.219757915C=	GRCh37
NC_000002.10:g.219466159C=	NCBI36
NG_012179.1:g.17661C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1176C= MANE Select	ENSP00000258411.3:p.Cys392=
ENST00000258411.7:c.1176C=	ENSP00000258411.3:p.Cys392=
NM_025216.2:c.1176C=	NP_079492.2:p.Cys392=
XM_011511928.1:c.1125C=	XP_011510230.1:p.Cys375=
XM_011511929.1:c.1080C=	XP_011510231.1:p.Cys360=
XM_011511930.1:c.796C=	XP_011510232.1:p.Pro266=
XM_011511929.2:c.1080C=	XP_011510231.1:p.Cys360=
NM_025216.3:c.1176C= MANE Select	NP_079492.2:p.Cys392=