Canonical Allele Identifier: CA1328961563

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882274T= , CM000664.2:g.218882274T=	GRCh38
NC_000002.11:g.219746996T= , CM000664.1:g.219746996T=	GRCh37
NC_000002.10:g.219455240T=	NCBI36
NG_012179.1:g.6742T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.227T= MANE Select	ENSP00000258411.3:p.Val76=
ENST00000258411.7:c.227T=	ENSP00000258411.3:p.Val76=
ENST00000458582.1:c.114T=
NM_025216.2:c.227T=	NP_079492.2:p.Val76=
XM_011511928.1:c.176T=	XP_011510230.1:p.Val59=
XM_011511929.1:c.131T=	XP_011510231.1:p.Val44=
XM_011511930.1:c.227T=	XP_011510232.1:p.Val76=
XM_011511929.2:c.131T=	XP_011510231.1:p.Val44=
NM_025216.3:c.227T= MANE Select	NP_079492.2:p.Val76=