Canonical Allele Identifier: CA1328965150

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890267C= , CM000664.2:g.218890267C=	GRCh38
NC_000002.11:g.219754989C= , CM000664.1:g.219754989C=	GRCh37
NC_000002.10:g.219463233C=	NCBI36
NG_012179.1:g.14735C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.660C= MANE Select	ENSP00000258411.3:p.Phe220=
ENST00000258411.7:c.660C=	ENSP00000258411.3:p.Phe220=
ENST00000458582.1:c.264-2507C=
NM_025216.2:c.660C=	NP_079492.2:p.Phe220=
XM_011511928.1:c.609C=	XP_011510230.1:p.Phe203=
XM_011511929.1:c.564C=	XP_011510231.1:p.Phe188=
XM_011511930.1:c.377-2507C=	XP_011510232.1:n.377-2507C=
XM_011511929.2:c.564C=	XP_011510231.1:p.Phe188=
NM_025216.3:c.660C= MANE Select	NP_079492.2:p.Phe220=