Canonical Allele Identifier: CA1955232872

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612297_17612318delinsGGGGACCGCTGCTGCCCACTCT , CM000673.2:g.17612297_17612318delinsGGGGACCGCTGCTGCCCACTCT	GRCh38
NC_000011.9:g.17633844_17633865delinsGGGGACCGCTGCTGCCCACTCT , CM000673.1:g.17633844_17633865delinsGGGGACCGCTGCTGCCCACTCT	GRCh37
NC_000011.8:g.17590420_17590441delinsGGGGACCGCTGCTGCCCACTCT	NCBI36
NG_033191.1:g.69925_69946delinsGGGGACCGCTGCTGCCCACTCT
NG_033191.2:g.69925_69946delinsGGGGACCGCTGCTGCCCACTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6295_6316delinsGGGGACCGCTGCTGCCCACTCT	ENSP00000382323.2:p.Gly2099=
ENST00000399397.6:c.6259_6280delinsGGGGACCGCTGCTGCCCACTCT MANE Select	ENSP00000382329.2:p.Gly2087=
ENST00000342528.2:c.3313_3334delinsGGGGACCGCTGCTGCCCACTCT	ENSP00000341666.2:p.Gly1105=
ENST00000399391.6:c.6295_6316delinsGGGGACCGCTGCTGCCCACTCT	ENSP00000382323.2:p.Gly2099=
ENST00000399397.5:c.6259_6280delinsGGGGACCGCTGCTGCCCACTCT	ENSP00000382329.2:p.Gly2087=
NM_001277269.1:c.6295_6316delinsGGGGACCGCTGCTGCCCACTCT	NP_001264198.1:p.Gly2099=
NM_001292063.1:c.6259_6280delinsGGGGACCGCTGCTGCCCACTCT	NP_001278992.1:p.Gly2087=
NM_001277269.2:c.6295_6316delinsGGGGACCGCTGCTGCCCACTCT	NP_001264198.1:p.Gly2099=
NM_001292063.2:c.6259_6280delinsGGGGACCGCTGCTGCCCACTCT MANE Select	NP_001278992.1:p.Gly2087=