Canonical Allele Identifier: CA2612689947

Gene: OTOG

Linked Data

• gnomAD v4: 11-17634978-G-GGGGGGGGGGGGGGGGGGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634978_17634979insGGGGGGGGGGGGGGGGGGGC , CM000673.2:g.17634978_17634979insGGGGGGGGGGGGGGGGGGGC	GRCh38
NC_000011.9:g.17656525_17656526insGGGGGGGGGGGGGGGGGGGC , CM000673.1:g.17656525_17656526insGGGGGGGGGGGGGGGGGGGC	GRCh37
NC_000011.8:g.17613101_17613102insGGGGGGGGGGGGGGGGGGGC	NCBI36
NG_033191.1:g.92606_92607insGGGGGGGGGGGGGGGGGGGC
NG_033191.2:g.92606_92607insGGGGGGGGGGGGGGGGGGGC

Transcript Alleles

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