Canonical Allele Identifier: CA1328965662

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893256C= , CM000664.2:g.218893256C=	GRCh38
NC_000002.11:g.219757978C= , CM000664.1:g.219757978C=	GRCh37
NC_000002.10:g.219466222C=	NCBI36
NG_012179.1:g.17724C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1239C= MANE Select	ENSP00000258411.3:p.Val413=
ENST00000258411.7:c.1239C=	ENSP00000258411.3:p.Val413=
ENST00000489887.1:n.36C=
NM_025216.2:c.1239C=	NP_079492.2:p.Val413=
XM_011511928.1:c.1188C=	XP_011510230.1:p.Val396=
XM_011511929.1:c.1143C=	XP_011510231.1:p.Val381=
XM_011511930.1:c.859C=	XP_011510232.1:p.Gln287=
XM_011511929.2:c.1143C=	XP_011510231.1:p.Val381=
NM_025216.3:c.1239C= MANE Select	NP_079492.2:p.Val413=