Canonical Allele Identifier: CA1955197764

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553421G= , CM000673.2:g.17553421G=	GRCh38
NC_000011.9:g.17574968G= , CM000673.1:g.17574968G=	GRCh37
NC_000011.8:g.17531544G=	NCBI36
NG_033191.1:g.11049G=
NG_033191.2:g.11049G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.478G=	ENSP00000382323.2:p.Val160=
ENST00000399397.6:c.442G= MANE Select	ENSP00000382329.2:p.Val148=
ENST00000399391.6:c.478G=	ENSP00000382323.2:p.Val160=
ENST00000399397.5:c.442G=	ENSP00000382329.2:p.Val148=
ENST00000428619.1:c.259G=	ENSP00000399057.2:p.Val87=
ENST00000498332.5:n.348G=
NM_001277269.1:c.478G=	NP_001264198.1:p.Val160=
NM_001292063.1:c.442G=	NP_001278992.1:p.Val148=
NM_001277269.2:c.478G=	NP_001264198.1:p.Val160=
NM_001292063.2:c.442G= MANE Select	NP_001278992.1:p.Val148=