Canonical Allele Identifier: CA2612689781

Gene: OTOG

Linked Data

• gnomAD v4: 11-17634964-T-TCGGGGCGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634964_17634965insCGGGGCGGGGGGG , CM000673.2:g.17634964_17634965insCGGGGCGGGGGGG	GRCh38
NC_000011.9:g.17656511_17656512insCGGGGCGGGGGGG , CM000673.1:g.17656511_17656512insCGGGGCGGGGGGG	GRCh37
NC_000011.8:g.17613087_17613088insCGGGGCGGGGGGG	NCBI36
NG_033191.1:g.92592_92593insCGGGGCGGGGGGG
NG_033191.2:g.92592_92593insCGGGGCGGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7621+16_7621+17insCGGGGCGGGGGGG	ENSP00000382323.2:n.7621+16_7621+17insCGGGGCGGGGGGG
ENST00000399397.6:c.7585+16_7585+17insCGGGGCGGGGGGG MANE Select	ENSP00000382329.2:n.7585+16_7585+17insCGGGGCGGGGGGG
ENST00000342528.2:c.4322-646_4322-645insCGGGGCGGGGGGG	ENSP00000341666.2:n.4322-646_4322-645insCGGGGCGGGGGGG
ENST00000399391.6:c.7621+16_7621+17insCGGGGCGGGGGGG	ENSP00000382323.2:n.7621+16_7621+17insCGGGGCGGGGGGG
ENST00000399397.5:c.7585+16_7585+17insCGGGGCGGGGGGG	ENSP00000382329.2:n.7585+16_7585+17insCGGGGCGGGGGGG
NM_001277269.1:c.7621+16_7621+17insCGGGGCGGGGGGG	NP_001264198.1:n.7621+16_7621+17insCGGGGCGGGGGGG
NM_001292063.1:c.7585+16_7585+17insCGGGGCGGGGGGG	NP_001278992.1:n.7585+16_7585+17insCGGGGCGGGGGGG
NM_001277269.2:c.7621+16_7621+17insCGGGGCGGGGGGG	NP_001264198.1:n.7621+16_7621+17insCGGGGCGGGGGGG
NM_001292063.2:c.7585+16_7585+17insCGGGGCGGGGGGG MANE Select	NP_001278992.1:n.7585+16_7585+17insCGGGGCGGGGGGG