Canonical Allele Identifier: CA1328961300

Gene: WNT10A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218881698_218881700delinsCTT , CM000664.2:g.218881698_218881700delinsCTT	GRCh38
NC_000002.11:g.219746420_219746422delinsCTT , CM000664.1:g.219746420_219746422delinsCTT	GRCh37
NC_000002.10:g.219454664_219454666delinsCTT	NCBI36
NG_012179.1:g.6166_6168delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258411.8:c.114-463_114-461delinsCTT MANE Select	ENSP00000258411.3:n.114-463_114-461delinsCTT
ENST00000258411.7:c.114-463_114-461delinsCTT	ENSP00000258411.3:n.114-463_114-461delinsCTT
NM_025216.2:c.114-463_114-461delinsCTT	NP_079492.2:n.114-463_114-461delinsCTT
XM_011511928.1:c.62+231_62+233delinsCTT	XP_011510230.1:n.62+231_62+233delinsCTT
XM_011511929.1:c.18-463_18-461delinsCTT	XP_011510231.1:n.18-463_18-461delinsCTT
XM_011511930.1:c.114-463_114-461delinsCTT	XP_011510232.1:n.114-463_114-461delinsCTT
XM_011511929.2:c.18-463_18-461delinsCTT	XP_011510231.1:n.18-463_18-461delinsCTT
NM_025216.3:c.114-463_114-461delinsCTT MANE Select	NP_079492.2:n.114-463_114-461delinsCTT