Canonical Allele Identifier: CA2612689709

Gene: OTOG

Linked Data

• gnomAD v4: 11-17634964-T-TGGTGTGGGGCCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634966_17634967insTGTGGGGCCGGGG , CM000673.2:g.17634966_17634967insTGTGGGGCCGGGG	GRCh38
NC_000011.9:g.17656513_17656514insTGTGGGGCCGGGG , CM000673.1:g.17656513_17656514insTGTGGGGCCGGGG	GRCh37
NC_000011.8:g.17613089_17613090insTGTGGGGCCGGGG	NCBI36
NG_033191.1:g.92594_92595insTGTGGGGCCGGGG
NG_033191.2:g.92594_92595insTGTGGGGCCGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7621+18_7621+19insTGTGGGGCCGGGG	ENSP00000382323.2:n.7621+18_7621+19insTGTGGGGCCGGGG
ENST00000399397.6:c.7585+18_7585+19insTGTGGGGCCGGGG MANE Select	ENSP00000382329.2:n.7585+18_7585+19insTGTGGGGCCGGGG
ENST00000342528.2:c.4322-644_4322-643insTGTGGGGCCGGGG	ENSP00000341666.2:n.4322-644_4322-643insTGTGGGGCCGGGG
ENST00000399391.6:c.7621+18_7621+19insTGTGGGGCCGGGG	ENSP00000382323.2:n.7621+18_7621+19insTGTGGGGCCGGGG
ENST00000399397.5:c.7585+18_7585+19insTGTGGGGCCGGGG	ENSP00000382329.2:n.7585+18_7585+19insTGTGGGGCCGGGG
NM_001277269.1:c.7621+18_7621+19insTGTGGGGCCGGGG	NP_001264198.1:n.7621+18_7621+19insTGTGGGGCCGGGG
NM_001292063.1:c.7585+18_7585+19insTGTGGGGCCGGGG	NP_001278992.1:n.7585+18_7585+19insTGTGGGGCCGGGG
NM_001277269.2:c.7621+18_7621+19insTGTGGGGCCGGGG	NP_001264198.1:n.7621+18_7621+19insTGTGGGGCCGGGG
NM_001292063.2:c.7585+18_7585+19insTGTGGGGCCGGGG MANE Select	NP_001278992.1:n.7585+18_7585+19insTGTGGGGCCGGGG