Canonical Allele Identifier: CA2592430262

Gene: OTOG

Linked Data

• gnomAD v3: 11-17634964-T-TGGGGGGGGGGGG
• gnomAD v4: 11-17634964-T-TGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634968_17634969insGGGGGGGGGGGG , CM000673.2:g.17634968_17634969insGGGGGGGGGGGG	GRCh38
NC_000011.9:g.17656515_17656516insGGGGGGGGGGGG , CM000673.1:g.17656515_17656516insGGGGGGGGGGGG	GRCh37
NC_000011.8:g.17613091_17613092insGGGGGGGGGGGG	NCBI36
NG_033191.1:g.92596_92597insGGGGGGGGGGGG
NG_033191.2:g.92596_92597insGGGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7621+20_7621+21insGGGGGGGGGGGG	ENSP00000382323.2:n.7621+20_7621+21insGGGGGGGGGGGG
ENST00000399397.6:c.7585+20_7585+21insGGGGGGGGGGGG MANE Select	ENSP00000382329.2:n.7585+20_7585+21insGGGGGGGGGGGG
ENST00000342528.2:c.4322-642_4322-641insGGGGGGGGGGGG	ENSP00000341666.2:n.4322-642_4322-641insGGGGGGGGGGGG
ENST00000399391.6:c.7621+20_7621+21insGGGGGGGGGGGG	ENSP00000382323.2:n.7621+20_7621+21insGGGGGGGGGGGG
ENST00000399397.5:c.7585+20_7585+21insGGGGGGGGGGGG	ENSP00000382329.2:n.7585+20_7585+21insGGGGGGGGGGGG
NM_001277269.1:c.7621+20_7621+21insGGGGGGGGGGGG	NP_001264198.1:n.7621+20_7621+21insGGGGGGGGGGGG
NM_001292063.1:c.7585+20_7585+21insGGGGGGGGGGGG	NP_001278992.1:n.7585+20_7585+21insGGGGGGGGGGGG
NM_001277269.2:c.7621+20_7621+21insGGGGGGGGGGGG	NP_001264198.1:n.7621+20_7621+21insGGGGGGGGGGGG
NM_001292063.2:c.7585+20_7585+21insGGGGGGGGGGGG MANE Select	NP_001278992.1:n.7585+20_7585+21insGGGGGGGGGGGG