Canonical Allele Identifier: CA1955197549

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553030T= , CM000673.2:g.17553030T=	GRCh38
NC_000011.9:g.17574577T= , CM000673.1:g.17574577T=	GRCh37
NC_000011.8:g.17531153T=	NCBI36
NG_033191.1:g.10658T=
NG_033191.2:g.10658T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.329-89T=	ENSP00000382323.2:n.329-89T=
ENST00000399397.6:c.293-89T= MANE Select	ENSP00000382329.2:n.293-89T=
ENST00000399391.6:c.329-89T=	ENSP00000382323.2:n.329-89T=
ENST00000399397.5:c.293-89T=	ENSP00000382329.2:n.293-89T=
ENST00000428619.1:c.110-89T=	ENSP00000399057.2:n.110-89T=
ENST00000498332.5:n.199-89T=
NM_001277269.1:c.329-89T=	NP_001264198.1:n.329-89T=
NM_001292063.1:c.293-89T=	NP_001278992.1:n.293-89T=
NM_001277269.2:c.329-89T=	NP_001264198.1:n.329-89T=
NM_001292063.2:c.293-89T= MANE Select	NP_001278992.1:n.293-89T=