Canonical Allele Identifier: CA2612689652

Gene: OTOG

Linked Data

• gnomAD v4: 11-17634964-T-TGGGTTGGGCCGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634967_17634968insTTGGGCCGGGGGGGGGG , CM000673.2:g.17634967_17634968insTTGGGCCGGGGGGGGGG	GRCh38
NC_000011.9:g.17656514_17656515insTTGGGCCGGGGGGGGGG , CM000673.1:g.17656514_17656515insTTGGGCCGGGGGGGGGG	GRCh37
NC_000011.8:g.17613090_17613091insTTGGGCCGGGGGGGGGG	NCBI36
NG_033191.1:g.92595_92596insTTGGGCCGGGGGGGGGG
NG_033191.2:g.92595_92596insTTGGGCCGGGGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7621+19_7621+20insTTGGGCCGGGGGGGGGG	ENSP00000382323.2:n.7621+19_7621+20insTTGGGCCGGGGGGGGGG
ENST00000399397.6:c.7585+19_7585+20insTTGGGCCGGGGGGGGGG MANE Select	ENSP00000382329.2:n.7585+19_7585+20insTTGGGCCGGGGGGGGGG
ENST00000342528.2:c.4322-643_4322-642insTTGGGCCGGGGGGGGGG	ENSP00000341666.2:n.4322-643_4322-642insTTGGGCCGGGGGGGGGG
ENST00000399391.6:c.7621+19_7621+20insTTGGGCCGGGGGGGGGG	ENSP00000382323.2:n.7621+19_7621+20insTTGGGCCGGGGGGGGGG
ENST00000399397.5:c.7585+19_7585+20insTTGGGCCGGGGGGGGGG	ENSP00000382329.2:n.7585+19_7585+20insTTGGGCCGGGGGGGGGG
NM_001277269.1:c.7621+19_7621+20insTTGGGCCGGGGGGGGGG	NP_001264198.1:n.7621+19_7621+20insTTGGGCCGGGGGGGGGG
NM_001292063.1:c.7585+19_7585+20insTTGGGCCGGGGGGGGGG	NP_001278992.1:n.7585+19_7585+20insTTGGGCCGGGGGGGGGG
NM_001277269.2:c.7621+19_7621+20insTTGGGCCGGGGGGGGGG	NP_001264198.1:n.7621+19_7621+20insTTGGGCCGGGGGGGGGG
NM_001292063.2:c.7585+19_7585+20insTTGGGCCGGGGGGGGGG MANE Select	NP_001278992.1:n.7585+19_7585+20insTTGGGCCGGGGGGGGGG