Canonical Allele Identifier: CA1328965652

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218893246C= , CM000664.2:g.218893246C=	GRCh38
NC_000002.11:g.219757968C= , CM000664.1:g.219757968C=	GRCh37
NC_000002.10:g.219466212C=	NCBI36
NG_012179.1:g.17714C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.1229C= MANE Select	ENSP00000258411.3:p.Thr410=
ENST00000258411.7:c.1229C=	ENSP00000258411.3:p.Thr410=
ENST00000489887.1:n.26C=
NM_025216.2:c.1229C=	NP_079492.2:p.Thr410=
XM_011511928.1:c.1178C=	XP_011510230.1:p.Thr393=
XM_011511929.1:c.1133C=	XP_011510231.1:p.Thr378=
XM_011511930.1:c.849C=	XP_011510232.1:p.His283=
XM_011511929.2:c.1133C=	XP_011510231.1:p.Thr378=
NM_025216.3:c.1229C= MANE Select	NP_079492.2:p.Thr410=