Canonical Allele Identifier: CA1328961510

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882161G= , CM000664.2:g.218882161G=	GRCh38
NC_000002.11:g.219746883G= , CM000664.1:g.219746883G=	GRCh37
NC_000002.10:g.219455127G=	NCBI36
NG_012179.1:g.6629G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114G= MANE Select	ENSP00000258411.3:p.Arg38=
ENST00000258411.7:c.114G=	ENSP00000258411.3:p.Arg38=
ENST00000458582.1:c.1G=
NM_025216.2:c.114G=	NP_079492.2:p.Arg38=
XM_011511928.1:c.63G=	XP_011510230.1:p.Arg21=
XM_011511929.1:c.18G=	XP_011510231.1:p.Arg6=
XM_011511930.1:c.114G=	XP_011510232.1:p.Arg38=
XM_011511929.2:c.18G=	XP_011510231.1:p.Arg6=
NM_025216.3:c.114G= MANE Select	NP_079492.2:p.Arg38=