Canonical Allele Identifier: CA1328965598

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893205C= , CM000664.2:g.218893205C=	GRCh38
NC_000002.11:g.219757927C= , CM000664.1:g.219757927C=	GRCh37
NC_000002.10:g.219466171C=	NCBI36
NG_012179.1:g.17673C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1188C= MANE Select	ENSP00000258411.3:p.Phe396=
ENST00000258411.7:c.1188C=	ENSP00000258411.3:p.Phe396=
NM_025216.2:c.1188C=	NP_079492.2:p.Phe396=
XM_011511928.1:c.1137C=	XP_011510230.1:p.Phe379=
XM_011511929.1:c.1092C=	XP_011510231.1:p.Phe364=
XM_011511930.1:c.808C=	XP_011510232.1:p.Pro270=
XM_011511929.2:c.1092C=	XP_011510231.1:p.Phe364=
NM_025216.3:c.1188C= MANE Select	NP_079492.2:p.Phe396=