Canonical Allele Identifier: CA1955197770

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553432T= , CM000673.2:g.17553432T=	GRCh38
NC_000011.9:g.17574979T= , CM000673.1:g.17574979T=	GRCh37
NC_000011.8:g.17531555T=	NCBI36
NG_033191.1:g.11060T=
NG_033191.2:g.11060T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.489T=	ENSP00000382323.2:p.Phe163=
ENST00000399397.6:c.453T= MANE Select	ENSP00000382329.2:p.Phe151=
ENST00000399391.6:c.489T=	ENSP00000382323.2:p.Phe163=
ENST00000399397.5:c.453T=	ENSP00000382329.2:p.Phe151=
ENST00000428619.1:c.270T=	ENSP00000399057.2:p.Phe90=
ENST00000498332.5:n.359T=
NM_001277269.1:c.489T=	NP_001264198.1:p.Phe163=
NM_001292063.1:c.453T=	NP_001278992.1:p.Phe151=
NM_001277269.2:c.489T=	NP_001264198.1:p.Phe163=
NM_001292063.2:c.453T= MANE Select	NP_001278992.1:p.Phe151=