Canonical Allele Identifier: CA1328961557

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882259A= , CM000664.2:g.218882259A=	GRCh38
NC_000002.11:g.219746981A= , CM000664.1:g.219746981A=	GRCh37
NC_000002.10:g.219455225A=	NCBI36
NG_012179.1:g.6727A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.212A= MANE Select	ENSP00000258411.3:p.Gln71=
ENST00000258411.7:c.212A=	ENSP00000258411.3:p.Gln71=
ENST00000458582.1:c.99A=
NM_025216.2:c.212A=	NP_079492.2:p.Gln71=
XM_011511928.1:c.161A=	XP_011510230.1:p.Gln54=
XM_011511929.1:c.116A=	XP_011510231.1:p.Gln39=
XM_011511930.1:c.212A=	XP_011510232.1:p.Gln71=
XM_011511929.2:c.116A=	XP_011510231.1:p.Gln39=
NM_025216.3:c.212A= MANE Select	NP_079492.2:p.Gln71=