Canonical Allele Identifier: CA2612690287

Gene: OTOG

Linked Data

• gnomAD v4: 11-17635193-TCGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635198_17635200del , CM000673.2:g.17635198_17635200del	GRCh38
NC_000011.9:g.17656745_17656747del , CM000673.1:g.17656745_17656747del	GRCh37
NC_000011.8:g.17613321_17613323del	NCBI36
NG_033191.1:g.92826_92828del
NG_033191.2:g.92826_92828del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7729+11_7729+13del	ENSP00000382323.2:n.7729+11_7729+13del
ENST00000399397.6:c.7693+11_7693+13del MANE Select	ENSP00000382329.2:n.7693+11_7693+13del
ENST00000342528.2:c.4322-412_4322-410del	ENSP00000341666.2:n.4322-412_4322-410del
ENST00000399391.6:c.7729+11_7729+13del	ENSP00000382323.2:n.7729+11_7729+13del
ENST00000399397.5:c.7693+11_7693+13del	ENSP00000382329.2:n.7693+11_7693+13del
NM_001277269.1:c.7729+11_7729+13del	NP_001264198.1:n.7729+11_7729+13del
NM_001292063.1:c.7693+11_7693+13del	NP_001278992.1:n.7693+11_7693+13del
NM_001277269.2:c.7729+11_7729+13del	NP_001264198.1:n.7729+11_7729+13del
NM_001292063.2:c.7693+11_7693+13del MANE Select	NP_001278992.1:n.7693+11_7693+13del