Canonical Allele Identifier: CA2574771139

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634978_17634979insGGGT , CM000673.2:g.17634978_17634979insGGGT	GRCh38
NC_000011.9:g.17656525_17656526insGGGT , CM000673.1:g.17656525_17656526insGGGT	GRCh37
NC_000011.8:g.17613101_17613102insGGGT	NCBI36
NG_033191.1:g.92606_92607insGGGT
NG_033191.2:g.92606_92607insGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7621+30_7621+31insGGGT	ENSP00000382323.2:n.7621+30_7621+31insGGGT
ENST00000399397.6:c.7585+30_7585+31insGGGT MANE Select	ENSP00000382329.2:n.7585+30_7585+31insGGGT
ENST00000342528.2:c.4322-632_4322-631insGGGT	ENSP00000341666.2:n.4322-632_4322-631insGGGT
ENST00000399391.6:c.7621+30_7621+31insGGGT	ENSP00000382323.2:n.7621+30_7621+31insGGGT
ENST00000399397.5:c.7585+30_7585+31insGGGT	ENSP00000382329.2:n.7585+30_7585+31insGGGT
NM_001277269.1:c.7621+30_7621+31insGGGT	NP_001264198.1:n.7621+30_7621+31insGGGT
NM_001292063.1:c.7585+30_7585+31insGGGT	NP_001278992.1:n.7585+30_7585+31insGGGT
NM_001277269.2:c.7621+30_7621+31insGGGT	NP_001264198.1:n.7621+30_7621+31insGGGT
NM_001292063.2:c.7585+30_7585+31insGGGT MANE Select	NP_001278992.1:n.7585+30_7585+31insGGGT