Canonical Allele Identifier: CA1955197605

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553144C= , CM000673.2:g.17553144C=	GRCh38
NC_000011.9:g.17574691C= , CM000673.1:g.17574691C=	GRCh37
NC_000011.8:g.17531267C=	NCBI36
NG_033191.1:g.10772C=
NG_033191.2:g.10772C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.354C=	ENSP00000382323.2:p.Gly118=
ENST00000399397.6:c.318C= MANE Select	ENSP00000382329.2:p.Gly106=
ENST00000399391.6:c.354C=	ENSP00000382323.2:p.Gly118=
ENST00000399397.5:c.318C=	ENSP00000382329.2:p.Gly106=
ENST00000428619.1:c.135C=	ENSP00000399057.2:p.Gly45=
ENST00000498332.5:n.224C=
NM_001277269.1:c.354C=	NP_001264198.1:p.Gly118=
NM_001292063.1:c.318C=	NP_001278992.1:p.Gly106=
NM_001277269.2:c.354C=	NP_001264198.1:p.Gly118=
NM_001292063.2:c.318C= MANE Select	NP_001278992.1:p.Gly106=