Canonical Allele Identifier: CA2612689369

Gene: OTOG

Linked Data

• gnomAD v4: 11-17634886-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634889del , CM000673.2:g.17634889del	GRCh38
NC_000011.9:g.17656436del , CM000673.1:g.17656436del	GRCh37
NC_000011.8:g.17613012del	NCBI36
NG_033191.1:g.92517del
NG_033191.2:g.92517del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7562del	ENSP00000382323.2:p.Pro2521GlnfsTer?
ENST00000399397.6:c.7526del MANE Select	ENSP00000382329.2:p.Pro2509GlnfsTer?
ENST00000342528.2:c.4322-721del	ENSP00000341666.2:n.4322-721del
ENST00000399391.6:c.7562del	ENSP00000382323.2:p.Pro2521GlnfsTer?
ENST00000399397.5:c.7526del	ENSP00000382329.2:p.Pro2509GlnfsTer?
NM_001277269.1:c.7562del	NP_001264198.1:p.Pro2521GlnfsTer?
NM_001292063.1:c.7526del	NP_001278992.1:p.Pro2509GlnfsTer?
NM_001277269.2:c.7562del	NP_001264198.1:p.Pro2521GlnfsTer?
NM_001292063.2:c.7526del MANE Select	NP_001278992.1:p.Pro2509GlnfsTer?