Canonical Allele Identifier: CA1328965633

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893229C= , CM000664.2:g.218893229C=	GRCh38
NC_000002.11:g.219757951C= , CM000664.1:g.219757951C=	GRCh37
NC_000002.10:g.219466195C=	NCBI36
NG_012179.1:g.17697C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1212C= MANE Select	ENSP00000258411.3:p.Cys404=
ENST00000258411.7:c.1212C=	ENSP00000258411.3:p.Cys404=
ENST00000489887.1:n.9C=
NM_025216.2:c.1212C=	NP_079492.2:p.Cys404=
XM_011511928.1:c.1161C=	XP_011510230.1:p.Cys387=
XM_011511929.1:c.1116C=	XP_011510231.1:p.Cys372=
XM_011511930.1:c.832C=	XP_011510232.1:p.Arg278=
XM_011511929.2:c.1116C=	XP_011510231.1:p.Cys372=
NM_025216.3:c.1212C= MANE Select	NP_079492.2:p.Cys404=