Canonical Allele Identifier: CA1955197538

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553011G= , CM000673.2:g.17553011G=	GRCh38
NC_000011.9:g.17574558G= , CM000673.1:g.17574558G=	GRCh37
NC_000011.8:g.17531134G=	NCBI36
NG_033191.1:g.10639G=
NG_033191.2:g.10639G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.329-108G=	ENSP00000382323.2:n.329-108G=
ENST00000399397.6:c.293-108G= MANE Select	ENSP00000382329.2:n.293-108G=
ENST00000399391.6:c.329-108G=	ENSP00000382323.2:n.329-108G=
ENST00000399397.5:c.293-108G=	ENSP00000382329.2:n.293-108G=
ENST00000428619.1:c.110-108G=	ENSP00000399057.2:n.110-108G=
ENST00000498332.5:n.199-108G=
NM_001277269.1:c.329-108G=	NP_001264198.1:n.329-108G=
NM_001292063.1:c.293-108G=	NP_001278992.1:n.293-108G=
NM_001277269.2:c.329-108G=	NP_001264198.1:n.329-108G=
NM_001292063.2:c.293-108G= MANE Select	NP_001278992.1:n.293-108G=