Canonical Allele Identifier: CA1955197751

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553394A= , CM000673.2:g.17553394A=	GRCh38
NC_000011.9:g.17574941A= , CM000673.1:g.17574941A=	GRCh37
NC_000011.8:g.17531517A=	NCBI36
NG_033191.1:g.11022A=
NG_033191.2:g.11022A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.451A=	ENSP00000382323.2:p.Ile151=
ENST00000399397.6:c.415A= MANE Select	ENSP00000382329.2:p.Ile139=
ENST00000399391.6:c.451A=	ENSP00000382323.2:p.Ile151=
ENST00000399397.5:c.415A=	ENSP00000382329.2:p.Ile139=
ENST00000428619.1:c.232A=	ENSP00000399057.2:p.Ile78=
ENST00000498332.5:n.321A=
NM_001277269.1:c.451A=	NP_001264198.1:p.Ile151=
NM_001292063.1:c.415A=	NP_001278992.1:p.Ile139=
NM_001277269.2:c.451A=	NP_001264198.1:p.Ile151=
NM_001292063.2:c.415A= MANE Select	NP_001278992.1:p.Ile139=