Canonical Allele Identifier: CA1328966184

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218891661C= , CM000664.2:g.218891661C=	GRCh38
NC_000002.11:g.219756383C= , CM000664.1:g.219756383C=	GRCh37
NC_000002.10:g.219464627C=	NCBI36
NG_012179.1:g.16129C=

Transcript Alleles

HGVS	Amino-acid Change
NM_025216.3:c.757-1113C= MANE Select	NP_079492.2:n.757-1113C=
ENST00000258411.8:c.757-1113C= MANE Select	ENSP00000258411.3:n.757-1113C=
NM_025216.2:c.757-1113C=	NP_079492.2:n.757-1113C=
ENST00000258411.7:c.757-1113C=	ENSP00000258411.3:n.757-1113C=
ENST00000458582.1:c.264-1113C=
XM_011511928.1:c.706-1113C=	XP_011510230.1:n.706-1113C=
XM_011511929.1:c.661-1113C=	XP_011510231.1:n.661-1113C=
XM_011511929.2:c.661-1113C=	XP_011510231.1:n.661-1113C=
XM_011511930.1:c.377-1113C=	XP_011510232.1:n.377-1113C=