Canonical Allele Identifier: CA1955197606

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553145G= , CM000673.2:g.17553145G=	GRCh38
NC_000011.9:g.17574692G= , CM000673.1:g.17574692G=	GRCh37
NC_000011.8:g.17531268G=	NCBI36
NG_033191.1:g.10773G=
NG_033191.2:g.10773G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.355G=	ENSP00000382323.2:p.Glu119=
ENST00000399397.6:c.319G= MANE Select	ENSP00000382329.2:p.Glu107=
ENST00000399391.6:c.355G=	ENSP00000382323.2:p.Glu119=
ENST00000399397.5:c.319G=	ENSP00000382329.2:p.Glu107=
ENST00000428619.1:c.136G=	ENSP00000399057.2:p.Glu46=
ENST00000498332.5:n.225G=
NM_001277269.1:c.355G=	NP_001264198.1:p.Glu119=
NM_001292063.1:c.319G=	NP_001278992.1:p.Glu107=
NM_001277269.2:c.355G=	NP_001264198.1:p.Glu119=
NM_001292063.2:c.319G= MANE Select	NP_001278992.1:p.Glu107=