Canonical Allele Identifier: CA2612688145

Gene: OTOG

Linked Data

• gnomAD v4: 11-17612292-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612295del , CM000673.2:g.17612295del	GRCh38
NC_000011.9:g.17633842del , CM000673.1:g.17633842del	GRCh37
NC_000011.8:g.17590418del	NCBI36
NG_033191.1:g.69923del
NG_033191.2:g.69923del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6293del	ENSP00000382323.2:p.Gly2098ValfsTer21
ENST00000399397.6:c.6257del MANE Select	ENSP00000382329.2:p.Gly2086ValfsTer21
ENST00000342528.2:c.3311del	ENSP00000341666.2:p.Gly1104ValfsTer21
ENST00000399391.6:c.6293del	ENSP00000382323.2:p.Gly2098ValfsTer21
ENST00000399397.5:c.6257del	ENSP00000382329.2:p.Gly2086ValfsTer21
NM_001277269.1:c.6293del	NP_001264198.1:p.Gly2098ValfsTer21
NM_001292063.1:c.6257del	NP_001278992.1:p.Gly2086ValfsTer21
NM_001277269.2:c.6293del	NP_001264198.1:p.Gly2098ValfsTer21
NM_001292063.2:c.6257del MANE Select	NP_001278992.1:p.Gly2086ValfsTer21