Canonical Allele Identifier: CA1328965520

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893174A= , CM000664.2:g.218893174A=	GRCh38
NC_000002.11:g.219757896A= , CM000664.1:g.219757896A=	GRCh37
NC_000002.10:g.219466140A=	NCBI36
NG_012179.1:g.17642A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1157A= MANE Select	ENSP00000258411.3:p.Gln386=
ENST00000258411.7:c.1157A=	ENSP00000258411.3:p.Gln386=
NM_025216.2:c.1157A=	NP_079492.2:p.Gln386=
XM_011511928.1:c.1106A=	XP_011510230.1:p.Gln369=
XM_011511929.1:c.1061A=	XP_011510231.1:p.Gln354=
XM_011511930.1:c.777A=	XP_011510232.1:p.Pro259=
XM_011511929.2:c.1061A=	XP_011510231.1:p.Gln354=
NM_025216.3:c.1157A= MANE Select	NP_079492.2:p.Gln386=