Canonical Allele Identifier: CA1328961403

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881952_218881956delinsCAGCT , CM000664.2:g.218881952_218881956delinsCAGCT	GRCh38
NC_000002.11:g.219746674_219746678delinsCAGCT , CM000664.1:g.219746674_219746678delinsCAGCT	GRCh37
NC_000002.10:g.219454918_219454922delinsCAGCT	NCBI36
NG_012179.1:g.6420_6424delinsCAGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-209_114-205delinsCAGCT MANE Select	ENSP00000258411.3:n.114-209_114-205delinsCAGCT
ENST00000258411.7:c.114-209_114-205delinsCAGCT	ENSP00000258411.3:n.114-209_114-205delinsCAGCT
NM_025216.2:c.114-209_114-205delinsCAGCT	NP_079492.2:n.114-209_114-205delinsCAGCT
XM_011511928.1:c.63-209_63-205delinsCAGCT	XP_011510230.1:n.63-209_63-205delinsCAGCT
XM_011511929.1:c.18-209_18-205delinsCAGCT	XP_011510231.1:n.18-209_18-205delinsCAGCT
XM_011511930.1:c.114-209_114-205delinsCAGCT	XP_011510232.1:n.114-209_114-205delinsCAGCT
XM_011511929.2:c.18-209_18-205delinsCAGCT	XP_011510231.1:n.18-209_18-205delinsCAGCT
NM_025216.3:c.114-209_114-205delinsCAGCT MANE Select	NP_079492.2:n.114-209_114-205delinsCAGCT