Canonical Allele Identifier: CA1955236934

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635111G= , CM000673.2:g.17635111G=	GRCh38
NC_000011.9:g.17656658G= , CM000673.1:g.17656658G=	GRCh37
NC_000011.8:g.17613234G=	NCBI36
NG_033191.1:g.92739G=
NG_033191.2:g.92739G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7653G=	ENSP00000382323.2:p.Leu2551=
ENST00000399397.6:c.7617G= MANE Select	ENSP00000382329.2:p.Leu2539=
ENST00000342528.2:c.4322-499G=	ENSP00000341666.2:n.4322-499G=
ENST00000399391.6:c.7653G=	ENSP00000382323.2:p.Leu2551=
ENST00000399397.5:c.7617G=	ENSP00000382329.2:p.Leu2539=
NM_001277269.1:c.7653G=	NP_001264198.1:p.Leu2551=
NM_001292063.1:c.7617G=	NP_001278992.1:p.Leu2539=
NM_001277269.2:c.7653G=	NP_001264198.1:p.Leu2551=
NM_001292063.2:c.7617G= MANE Select	NP_001278992.1:p.Leu2539=