Canonical Allele Identifier: CA2612679957

Gene: OTOG

Linked Data

• gnomAD v4: 11-17553626-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553628del , CM000673.2:g.17553628del	GRCh38
NC_000011.9:g.17575175del , CM000673.1:g.17575175del	GRCh37
NC_000011.8:g.17531751del	NCBI36
NG_033191.1:g.11256del
NG_033191.2:g.11256del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.576+109del	ENSP00000382323.2:n.576+109del
ENST00000399397.6:c.540+109del MANE Select	ENSP00000382329.2:n.540+109del
ENST00000399391.6:c.576+109del	ENSP00000382323.2:n.576+109del
ENST00000399397.5:c.540+109del	ENSP00000382329.2:n.540+109del
ENST00000498332.5:n.446+109del
NM_001277269.1:c.576+109del	NP_001264198.1:n.576+109del
NM_001292063.1:c.540+109del	NP_001278992.1:n.540+109del
NM_001277269.2:c.576+109del	NP_001264198.1:n.576+109del
NM_001292063.2:c.540+109del MANE Select	NP_001278992.1:n.540+109del