Canonical Allele Identifier: CA1328961287

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881679_218881681delinsCAT , CM000664.2:g.218881679_218881681delinsCAT	GRCh38
NC_000002.11:g.219746401_219746403delinsCAT , CM000664.1:g.219746401_219746403delinsCAT	GRCh37
NC_000002.10:g.219454645_219454647delinsCAT	NCBI36
NG_012179.1:g.6147_6149delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-482_114-480delinsCAT MANE Select	ENSP00000258411.3:n.114-482_114-480delinsCAT
ENST00000258411.7:c.114-482_114-480delinsCAT	ENSP00000258411.3:n.114-482_114-480delinsCAT
NM_025216.2:c.114-482_114-480delinsCAT	NP_079492.2:n.114-482_114-480delinsCAT
XM_011511928.1:c.62+212_62+214delinsCAT	XP_011510230.1:n.62+212_62+214delinsCAT
XM_011511929.1:c.18-482_18-480delinsCAT	XP_011510231.1:n.18-482_18-480delinsCAT
XM_011511930.1:c.114-482_114-480delinsCAT	XP_011510232.1:n.114-482_114-480delinsCAT
XM_011511929.2:c.18-482_18-480delinsCAT	XP_011510231.1:n.18-482_18-480delinsCAT
NM_025216.3:c.114-482_114-480delinsCAT MANE Select	NP_079492.2:n.114-482_114-480delinsCAT