Canonical Allele Identifier: CA1955236806

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634885C= , CM000673.2:g.17634885C=	GRCh38
NC_000011.9:g.17656432C= , CM000673.1:g.17656432C=	GRCh37
NC_000011.8:g.17613008C=	NCBI36
NG_033191.1:g.92513C=
NG_033191.2:g.92513C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7558C=	ENSP00000382323.2:p.Arg2520=
ENST00000399397.6:c.7522C= MANE Select	ENSP00000382329.2:p.Arg2508=
ENST00000342528.2:c.4322-725C=	ENSP00000341666.2:n.4322-725C=
ENST00000399391.6:c.7558C=	ENSP00000382323.2:p.Arg2520=
ENST00000399397.5:c.7522C=	ENSP00000382329.2:p.Arg2508=
NM_001277269.1:c.7558C=	NP_001264198.1:p.Arg2520=
NM_001292063.1:c.7522C=	NP_001278992.1:p.Arg2508=
NM_001277269.2:c.7558C=	NP_001264198.1:p.Arg2520=
NM_001292063.2:c.7522C= MANE Select	NP_001278992.1:p.Arg2508=