Canonical Allele Identifier: CA1955197689

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553271G= , CM000673.2:g.17553271G=	GRCh38
NC_000011.9:g.17574818G= , CM000673.1:g.17574818G=	GRCh37
NC_000011.8:g.17531394G=	NCBI36
NG_033191.1:g.10899G=
NG_033191.2:g.10899G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.421+60G=	ENSP00000382323.2:n.421+60G=
ENST00000399397.6:c.385+60G= MANE Select	ENSP00000382329.2:n.385+60G=
ENST00000399391.6:c.421+60G=	ENSP00000382323.2:n.421+60G=
ENST00000399397.5:c.385+60G=	ENSP00000382329.2:n.385+60G=
ENST00000428619.1:c.202+60G=	ENSP00000399057.2:n.202+60G=
ENST00000498332.5:n.291+60G=
NM_001277269.1:c.421+60G=	NP_001264198.1:n.421+60G=
NM_001292063.1:c.385+60G=	NP_001278992.1:n.385+60G=
NM_001277269.2:c.421+60G=	NP_001264198.1:n.421+60G=
NM_001292063.2:c.385+60G= MANE Select	NP_001278992.1:n.385+60G=