Canonical Allele Identifier: CA1955197728

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553345_17553347delinsTTC , CM000673.2:g.17553345_17553347delinsTTC	GRCh38
NC_000011.9:g.17574892_17574894delinsTTC , CM000673.1:g.17574892_17574894delinsTTC	GRCh37
NC_000011.8:g.17531468_17531470delinsTTC	NCBI36
NG_033191.1:g.10973_10975delinsTTC
NG_033191.2:g.10973_10975delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.422-20_422-18delinsTTC	ENSP00000382323.2:n.422-20_422-18delinsTTC
ENST00000399397.6:c.386-20_386-18delinsTTC MANE Select	ENSP00000382329.2:n.386-20_386-18delinsTTC
ENST00000399391.6:c.422-20_422-18delinsTTC	ENSP00000382323.2:n.422-20_422-18delinsTTC
ENST00000399397.5:c.386-20_386-18delinsTTC	ENSP00000382329.2:n.386-20_386-18delinsTTC
ENST00000428619.1:c.203-20_203-18delinsTTC	ENSP00000399057.2:n.203-20_203-18delinsTTC
ENST00000498332.5:n.292-20_292-18delinsTTC
NM_001277269.1:c.422-20_422-18delinsTTC	NP_001264198.1:n.422-20_422-18delinsTTC
NM_001292063.1:c.386-20_386-18delinsTTC	NP_001278992.1:n.386-20_386-18delinsTTC
NM_001277269.2:c.422-20_422-18delinsTTC	NP_001264198.1:n.422-20_422-18delinsTTC
NM_001292063.2:c.386-20_386-18delinsTTC MANE Select	NP_001278992.1:n.386-20_386-18delinsTTC