Canonical Allele Identifier: CA1328965587

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893200C= , CM000664.2:g.218893200C=	GRCh38
NC_000002.11:g.219757922C= , CM000664.1:g.219757922C=	GRCh37
NC_000002.10:g.219466166C=	NCBI36
NG_012179.1:g.17668C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1183C= MANE Select	ENSP00000258411.3:p.Arg395=
ENST00000258411.7:c.1183C=	ENSP00000258411.3:p.Arg395=
NM_025216.2:c.1183C=	NP_079492.2:p.Arg395=
XM_011511928.1:c.1132C=	XP_011510230.1:p.Arg378=
XM_011511929.1:c.1087C=	XP_011510231.1:p.Arg363=
XM_011511930.1:c.803C=	XP_011510232.1:p.Pro268=
XM_011511929.2:c.1087C=	XP_011510231.1:p.Arg363=
NM_025216.3:c.1183C= MANE Select	NP_079492.2:p.Arg395=