Canonical Allele Identifier: CA2612689889

Gene: OTOG

Linked Data

• gnomAD v4: 11-17634973-T-TGGGGGACGGGCTGAGGGCCGGGGGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634982_17634983insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG , CM000673.2:g.17634982_17634983insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG	GRCh38
NC_000011.9:g.17656529_17656530insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG , CM000673.1:g.17656529_17656530insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG	GRCh37
NC_000011.8:g.17613105_17613106insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG	NCBI36
NG_033191.1:g.92610_92611insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG
NG_033191.2:g.92610_92611insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7621+34_7621+35insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG	ENSP00000382323.2:n.7621+34_7621+35insGCTGAGGGCCGGGGGGGGGGGGG...
ENST00000399397.6:c.7585+34_7585+35insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG MANE Select	ENSP00000382329.2:n.7585+34_7585+35insGCTGAGGGCCGGGGGGGGGGGGG...
ENST00000342528.2:c.4322-628_4322-627insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG	ENSP00000341666.2:n.4322-628_4322-627insGCTGAGGGCCGGGGGGGGGGG...
ENST00000399391.6:c.7621+34_7621+35insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG	ENSP00000382323.2:n.7621+34_7621+35insGCTGAGGGCCGGGGGGGGGGGGG...
ENST00000399397.5:c.7585+34_7585+35insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG	ENSP00000382329.2:n.7585+34_7585+35insGCTGAGGGCCGGGGGGGGGGGGG...
NM_001277269.1:c.7621+34_7621+35insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG	NP_001264198.1:n.7621+34_7621+35insGCTGAGGGCCGGGGGGGGGGGGGGGG...
NM_001292063.1:c.7585+34_7585+35insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG	NP_001278992.1:n.7585+34_7585+35insGCTGAGGGCCGGGGGGGGGGGGGGGG...
NM_001277269.2:c.7621+34_7621+35insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG	NP_001264198.1:n.7621+34_7621+35insGCTGAGGGCCGGGGGGGGGGGGGGGG...
NM_001292063.2:c.7585+34_7585+35insGCTGAGGGCCGGGGGGGGGGGGGGGGGGGGGACGG MANE Select	NP_001278992.1:n.7585+34_7585+35insGCTGAGGGCCGGGGGGGGGGGGGGGG...