Canonical Allele Identifier: CA2612689701

Gene: OTOG

Linked Data

• gnomAD v4: 11-17634964-T-TGGTTTGGGCCCGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634966_17634967insTTTGGGCCCGGGGGGGG , CM000673.2:g.17634966_17634967insTTTGGGCCCGGGGGGGG	GRCh38
NC_000011.9:g.17656513_17656514insTTTGGGCCCGGGGGGGG , CM000673.1:g.17656513_17656514insTTTGGGCCCGGGGGGGG	GRCh37
NC_000011.8:g.17613089_17613090insTTTGGGCCCGGGGGGGG	NCBI36
NG_033191.1:g.92594_92595insTTTGGGCCCGGGGGGGG
NG_033191.2:g.92594_92595insTTTGGGCCCGGGGGGGG

Transcript Alleles

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