Canonical Allele Identifier: CA2612690342

Gene: OTOG

Linked Data

• gnomAD v4: 11-17635258-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635261del , CM000673.2:g.17635261del	GRCh38
NC_000011.9:g.17656808del , CM000673.1:g.17656808del	GRCh37
NC_000011.8:g.17613384del	NCBI36
NG_033191.1:g.92889del
NG_033191.2:g.92889del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7729+74del	ENSP00000382323.2:n.7729+74del
ENST00000399397.6:c.7693+74del MANE Select	ENSP00000382329.2:n.7693+74del
ENST00000342528.2:c.4322-349del	ENSP00000341666.2:n.4322-349del
ENST00000399391.6:c.7729+74del	ENSP00000382323.2:n.7729+74del
ENST00000399397.5:c.7693+74del	ENSP00000382329.2:n.7693+74del
NM_001277269.1:c.7729+74del	NP_001264198.1:n.7729+74del
NM_001292063.1:c.7693+74del	NP_001278992.1:n.7693+74del
NM_001277269.2:c.7729+74del	NP_001264198.1:n.7729+74del
NM_001292063.2:c.7693+74del MANE Select	NP_001278992.1:n.7693+74del