Canonical Allele Identifier: CA1328961535

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882213A= , CM000664.2:g.218882213A=	GRCh38
NC_000002.11:g.219746935A= , CM000664.1:g.219746935A=	GRCh37
NC_000002.10:g.219455179A=	NCBI36
NG_012179.1:g.6681A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.166A= MANE Select	ENSP00000258411.3:p.Asn56=
ENST00000258411.7:c.166A=	ENSP00000258411.3:p.Asn56=
ENST00000458582.1:c.53A=
NM_025216.2:c.166A=	NP_079492.2:p.Asn56=
XM_011511928.1:c.115A=	XP_011510230.1:p.Asn39=
XM_011511929.1:c.70A=	XP_011510231.1:p.Asn24=
XM_011511930.1:c.166A=	XP_011510232.1:p.Asn56=
XM_011511929.2:c.70A=	XP_011510231.1:p.Asn24=
NM_025216.3:c.166A= MANE Select	NP_079492.2:p.Asn56=