Canonical Allele Identifier: CA1955197632

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553199C= , CM000673.2:g.17553199C=	GRCh38
NC_000011.9:g.17574746C= , CM000673.1:g.17574746C=	GRCh37
NC_000011.8:g.17531322C=	NCBI36
NG_033191.1:g.10827C=
NG_033191.2:g.10827C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.409C=	ENSP00000382323.2:p.Arg137=
ENST00000399397.6:c.373C= MANE Select	ENSP00000382329.2:p.Arg125=
ENST00000399391.6:c.409C=	ENSP00000382323.2:p.Arg137=
ENST00000399397.5:c.373C=	ENSP00000382329.2:p.Arg125=
ENST00000428619.1:c.190C=	ENSP00000399057.2:p.Arg64=
ENST00000498332.5:n.279C=
NM_001277269.1:c.409C=	NP_001264198.1:p.Arg137=
NM_001292063.1:c.373C=	NP_001278992.1:p.Arg125=
NM_001277269.2:c.409C=	NP_001264198.1:p.Arg137=
NM_001292063.2:c.373C= MANE Select	NP_001278992.1:p.Arg125=