Canonical Allele Identifier: CA1328965550

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893185G= , CM000664.2:g.218893185G=	GRCh38
NC_000002.11:g.219757907G= , CM000664.1:g.219757907G=	GRCh37
NC_000002.10:g.219466151G=	NCBI36
NG_012179.1:g.17653G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1168G= MANE Select	ENSP00000258411.3:p.Glu390=
ENST00000258411.7:c.1168G=	ENSP00000258411.3:p.Glu390=
NM_025216.2:c.1168G=	NP_079492.2:p.Glu390=
XM_011511928.1:c.1117G=	XP_011510230.1:p.Glu373=
XM_011511929.1:c.1072G=	XP_011510231.1:p.Glu358=
XM_011511930.1:c.788G=	XP_011510232.1:p.Arg263=
XM_011511929.2:c.1072G=	XP_011510231.1:p.Glu358=
NM_025216.3:c.1168G= MANE Select	NP_079492.2:p.Glu390=