Canonical Allele Identifier: CA1955238556

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17638525C= , CM000673.2:g.17638525C=	GRCh38
NC_000011.9:g.17660072C= , CM000673.1:g.17660072C=	GRCh37
NC_000011.8:g.17616648C=	NCBI36
NG_033191.1:g.96153C=
NG_033191.2:g.96153C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7906C=	ENSP00000382323.2:p.Arg2636=
ENST00000399397.6:c.7870C= MANE Select	ENSP00000382329.2:p.Arg2624=
ENST00000342528.2:c.4498C=	ENSP00000341666.2:p.Arg1500=
ENST00000399391.6:c.7906C=	ENSP00000382323.2:p.Arg2636=
ENST00000399397.5:c.7870C=	ENSP00000382329.2:p.Arg2624=
NM_001277269.1:c.7906C=	NP_001264198.1:p.Arg2636=
NM_001292063.1:c.7870C=	NP_001278992.1:p.Arg2624=
NM_001277269.2:c.7906C=	NP_001264198.1:p.Arg2636=
NM_001292063.2:c.7870C= MANE Select	NP_001278992.1:p.Arg2624=