Canonical Allele Identifier: CA1328965527

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893178G= , CM000664.2:g.218893178G=	GRCh38
NC_000002.11:g.219757900G= , CM000664.1:g.219757900G=	GRCh37
NC_000002.10:g.219466144G=	NCBI36
NG_012179.1:g.17646G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1161G= MANE Select	ENSP00000258411.3:p.Thr387=
ENST00000258411.7:c.1161G=	ENSP00000258411.3:p.Thr387=
NM_025216.2:c.1161G=	NP_079492.2:p.Thr387=
XM_011511928.1:c.1110G=	XP_011510230.1:p.Thr370=
XM_011511929.1:c.1065G=	XP_011510231.1:p.Thr355=
XM_011511930.1:c.781G=	XP_011510232.1:p.Ala261=
XM_011511929.2:c.1065G=	XP_011510231.1:p.Thr355=
NM_025216.3:c.1161G= MANE Select	NP_079492.2:p.Thr387=