Canonical Allele Identifier: CA1955197753

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553400C= , CM000673.2:g.17553400C=	GRCh38
NC_000011.9:g.17574947C= , CM000673.1:g.17574947C=	GRCh37
NC_000011.8:g.17531523C=	NCBI36
NG_033191.1:g.11028C=
NG_033191.2:g.11028C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.457C=	ENSP00000382323.2:p.Arg153=
ENST00000399397.6:c.421C= MANE Select	ENSP00000382329.2:p.Arg141=
ENST00000399391.6:c.457C=	ENSP00000382323.2:p.Arg153=
ENST00000399397.5:c.421C=	ENSP00000382329.2:p.Arg141=
ENST00000428619.1:c.238C=	ENSP00000399057.2:p.Arg80=
ENST00000498332.5:n.327C=
NM_001277269.1:c.457C=	NP_001264198.1:p.Arg153=
NM_001292063.1:c.421C=	NP_001278992.1:p.Arg141=
NM_001277269.2:c.457C=	NP_001264198.1:p.Arg153=
NM_001292063.2:c.421C= MANE Select	NP_001278992.1:p.Arg141=