Canonical Allele Identifier: CA2612689800

Gene: OTOG

Linked Data

• gnomAD v4: 11-17634964-T-TGGGGTGGGCGCCGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634968_17634969insTGGGCGCCGGGGGGGGGGG , CM000673.2:g.17634968_17634969insTGGGCGCCGGGGGGGGGGG	GRCh38
NC_000011.9:g.17656515_17656516insTGGGCGCCGGGGGGGGGGG , CM000673.1:g.17656515_17656516insTGGGCGCCGGGGGGGGGGG	GRCh37
NC_000011.8:g.17613091_17613092insTGGGCGCCGGGGGGGGGGG	NCBI36
NG_033191.1:g.92596_92597insTGGGCGCCGGGGGGGGGGG
NG_033191.2:g.92596_92597insTGGGCGCCGGGGGGGGGGG

Transcript Alleles

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