Canonical Allele Identifier: CA1328961553

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882253G= , CM000664.2:g.218882253G=	GRCh38
NC_000002.11:g.219746975G= , CM000664.1:g.219746975G=	GRCh37
NC_000002.10:g.219455219G=	NCBI36
NG_012179.1:g.6721G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.206G= MANE Select	ENSP00000258411.3:p.Arg69=
ENST00000258411.7:c.206G=	ENSP00000258411.3:p.Arg69=
ENST00000458582.1:c.93G=
NM_025216.2:c.206G=	NP_079492.2:p.Arg69=
XM_011511928.1:c.155G=	XP_011510230.1:p.Arg52=
XM_011511929.1:c.110G=	XP_011510231.1:p.Arg37=
XM_011511930.1:c.206G=	XP_011510232.1:p.Arg69=
XM_011511929.2:c.110G=	XP_011510231.1:p.Arg37=
NM_025216.3:c.206G= MANE Select	NP_079492.2:p.Arg69=