Canonical Allele Identifier: CA1328965154

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890268G= , CM000664.2:g.218890268G=	GRCh38
NC_000002.11:g.219754990G= , CM000664.1:g.219754990G=	GRCh37
NC_000002.10:g.219463234G=	NCBI36
NG_012179.1:g.14736G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.661G= MANE Select	ENSP00000258411.3:p.Gly221=
ENST00000258411.7:c.661G=	ENSP00000258411.3:p.Gly221=
ENST00000458582.1:c.264-2506G=
NM_025216.2:c.661G=	NP_079492.2:p.Gly221=
XM_011511928.1:c.610G=	XP_011510230.1:p.Gly204=
XM_011511929.1:c.565G=	XP_011510231.1:p.Gly189=
XM_011511930.1:c.377-2506G=	XP_011510232.1:n.377-2506G=
XM_011511929.2:c.565G=	XP_011510231.1:p.Gly189=
NM_025216.3:c.661G= MANE Select	NP_079492.2:p.Gly221=