Canonical Allele Identifier: CA1955197765

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553422T= , CM000673.2:g.17553422T=	GRCh38
NC_000011.9:g.17574969T= , CM000673.1:g.17574969T=	GRCh37
NC_000011.8:g.17531545T=	NCBI36
NG_033191.1:g.11050T=
NG_033191.2:g.11050T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.479T=	ENSP00000382323.2:p.Val160=
ENST00000399397.6:c.443T= MANE Select	ENSP00000382329.2:p.Val148=
ENST00000399391.6:c.479T=	ENSP00000382323.2:p.Val160=
ENST00000399397.5:c.443T=	ENSP00000382329.2:p.Val148=
ENST00000428619.1:c.260T=	ENSP00000399057.2:p.Val87=
ENST00000498332.5:n.349T=
NM_001277269.1:c.479T=	NP_001264198.1:p.Val160=
NM_001292063.1:c.443T=	NP_001278992.1:p.Val148=
NM_001277269.2:c.479T=	NP_001264198.1:p.Val160=
NM_001292063.2:c.443T= MANE Select	NP_001278992.1:p.Val148=