Canonical Allele Identifier: CA1328965505

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893165T= , CM000664.2:g.218893165T=	GRCh38
NC_000002.11:g.219757887T= , CM000664.1:g.219757887T=	GRCh37
NC_000002.10:g.219466131T=	NCBI36
NG_012179.1:g.17633T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.1148T= MANE Select	ENSP00000258411.3:p.Ile383=
ENST00000258411.7:c.1148T=	ENSP00000258411.3:p.Ile383=
NM_025216.2:c.1148T=	NP_079492.2:p.Ile383=
XM_011511928.1:c.1097T=	XP_011510230.1:p.Ile366=
XM_011511929.1:c.1052T=	XP_011510231.1:p.Ile351=
XM_011511930.1:c.768T=	XP_011510232.1:p.His256=
XM_011511929.2:c.1052T=	XP_011510231.1:p.Ile351=
NM_025216.3:c.1148T= MANE Select	NP_079492.2:p.Ile383=