Canonical Allele Identifier: CA1955197603

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553142G= , CM000673.2:g.17553142G=	GRCh38
NC_000011.9:g.17574689G= , CM000673.1:g.17574689G=	GRCh37
NC_000011.8:g.17531265G=	NCBI36
NG_033191.1:g.10770G=
NG_033191.2:g.10770G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.352G=	ENSP00000382323.2:p.Gly118=
ENST00000399397.6:c.316G= MANE Select	ENSP00000382329.2:p.Gly106=
ENST00000399391.6:c.352G=	ENSP00000382323.2:p.Gly118=
ENST00000399397.5:c.316G=	ENSP00000382329.2:p.Gly106=
ENST00000428619.1:c.133G=	ENSP00000399057.2:p.Gly45=
ENST00000498332.5:n.222G=
NM_001277269.1:c.352G=	NP_001264198.1:p.Gly118=
NM_001292063.1:c.316G=	NP_001278992.1:p.Gly106=
NM_001277269.2:c.352G=	NP_001264198.1:p.Gly118=
NM_001292063.2:c.316G= MANE Select	NP_001278992.1:p.Gly106=