Canonical Allele Identifier: CA1328961522

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218882190G= , CM000664.2:g.218882190G=	GRCh38
NC_000002.11:g.219746912G= , CM000664.1:g.219746912G=	GRCh37
NC_000002.10:g.219455156G=	NCBI36
NG_012179.1:g.6658G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.143G= MANE Select	ENSP00000258411.3:p.Arg48=
ENST00000258411.7:c.143G=	ENSP00000258411.3:p.Arg48=
ENST00000458582.1:c.30G=
NM_025216.2:c.143G=	NP_079492.2:p.Arg48=
XM_011511928.1:c.92G=	XP_011510230.1:p.Arg31=
XM_011511929.1:c.47G=	XP_011510231.1:p.Arg16=
XM_011511930.1:c.143G=	XP_011510232.1:p.Arg48=
XM_011511929.2:c.47G=	XP_011510231.1:p.Arg16=
NM_025216.3:c.143G= MANE Select	NP_079492.2:p.Arg48=