Canonical Allele Identifier: CA2612679669

Gene: OTOG

Linked Data

• gnomAD v4: 11-17553461-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553464del , CM000673.2:g.17553464del	GRCh38
NC_000011.9:g.17575011del , CM000673.1:g.17575011del	GRCh37
NC_000011.8:g.17531587del	NCBI36
NG_033191.1:g.11092del
NG_033191.2:g.11092del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.521del	ENSP00000382323.2:p.Gly174AlafsTer?
ENST00000399397.6:c.485del MANE Select	ENSP00000382329.2:p.Gly162AlafsTer?
ENST00000399391.6:c.521del	ENSP00000382323.2:p.Gly174AlafsTer?
ENST00000399397.5:c.485del	ENSP00000382329.2:p.Gly162AlafsTer?
ENST00000498332.5:n.391del
NM_001277269.1:c.521del	NP_001264198.1:p.Gly174AlafsTer?
NM_001292063.1:c.485del	NP_001278992.1:p.Gly162AlafsTer?
NM_001277269.2:c.521del	NP_001264198.1:p.Gly174AlafsTer?
NM_001292063.2:c.485del MANE Select	NP_001278992.1:p.Gly162AlafsTer?