Canonical Allele Identifier: CA1955197750

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553392G= , CM000673.2:g.17553392G=	GRCh38
NC_000011.9:g.17574939G= , CM000673.1:g.17574939G=	GRCh37
NC_000011.8:g.17531515G=	NCBI36
NG_033191.1:g.11020G=
NG_033191.2:g.11020G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.449G=	ENSP00000382323.2:p.Ser150=
ENST00000399397.6:c.413G= MANE Select	ENSP00000382329.2:p.Ser138=
ENST00000399391.6:c.449G=	ENSP00000382323.2:p.Ser150=
ENST00000399397.5:c.413G=	ENSP00000382329.2:p.Ser138=
ENST00000428619.1:c.230G=	ENSP00000399057.2:p.Ser77=
ENST00000498332.5:n.319G=
NM_001277269.1:c.449G=	NP_001264198.1:p.Ser150=
NM_001292063.1:c.413G=	NP_001278992.1:p.Ser138=
NM_001277269.2:c.449G=	NP_001264198.1:p.Ser150=
NM_001292063.2:c.413G= MANE Select	NP_001278992.1:p.Ser138=