Canonical Allele Identifier: CA1328965128

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890257A= , CM000664.2:g.218890257A=	GRCh38
NC_000002.11:g.219754979A= , CM000664.1:g.219754979A=	GRCh37
NC_000002.10:g.219463223A=	NCBI36
NG_012179.1:g.14725A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.650A= MANE Select	ENSP00000258411.3:p.Asp217=
ENST00000258411.7:c.650A=	ENSP00000258411.3:p.Asp217=
ENST00000458582.1:c.264-2517A=
NM_025216.2:c.650A=	NP_079492.2:p.Asp217=
XM_011511928.1:c.599A=	XP_011510230.1:p.Asp200=
XM_011511929.1:c.554A=	XP_011510231.1:p.Asp185=
XM_011511930.1:c.377-2517A=	XP_011510232.1:n.377-2517A=
XM_011511929.2:c.554A=	XP_011510231.1:p.Asp185=
NM_025216.3:c.650A= MANE Select	NP_079492.2:p.Asp217=