Canonical Allele Identifier: CA1328965146

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218890263G= , CM000664.2:g.218890263G=	GRCh38
NC_000002.11:g.219754985G= , CM000664.1:g.219754985G=	GRCh37
NC_000002.10:g.219463229G=	NCBI36
NG_012179.1:g.14731G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000258411.8:c.656G= MANE Select	ENSP00000258411.3:p.Gly219=
ENST00000258411.7:c.656G=	ENSP00000258411.3:p.Gly219=
ENST00000458582.1:c.264-2511G=
NM_025216.2:c.656G=	NP_079492.2:p.Gly219=
XM_011511928.1:c.605G=	XP_011510230.1:p.Gly202=
XM_011511929.1:c.560G=	XP_011510231.1:p.Gly187=
XM_011511930.1:c.377-2511G=	XP_011510232.1:n.377-2511G=
XM_011511929.2:c.560G=	XP_011510231.1:p.Gly187=
NM_025216.3:c.656G= MANE Select	NP_079492.2:p.Gly219=