Canonical Allele Identifier: CA1955236980

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635193T= , CM000673.2:g.17635193T=	GRCh38
NC_000011.9:g.17656740T= , CM000673.1:g.17656740T=	GRCh37
NC_000011.8:g.17613316T=	NCBI36
NG_033191.1:g.92821T=
NG_033191.2:g.92821T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7729+6T=	ENSP00000382323.2:n.7729+6T=
ENST00000399397.6:c.7693+6T= MANE Select	ENSP00000382329.2:n.7693+6T=
ENST00000342528.2:c.4322-417T=	ENSP00000341666.2:n.4322-417T=
ENST00000399391.6:c.7729+6T=	ENSP00000382323.2:n.7729+6T=
ENST00000399397.5:c.7693+6T=	ENSP00000382329.2:n.7693+6T=
NM_001277269.1:c.7729+6T=	NP_001264198.1:n.7729+6T=
NM_001292063.1:c.7693+6T=	NP_001278992.1:n.7693+6T=
NM_001277269.2:c.7729+6T=	NP_001264198.1:n.7729+6T=
NM_001292063.2:c.7693+6T= MANE Select	NP_001278992.1:n.7693+6T=