Canonical Allele Identifier: CA1955232889

Gene: OTOG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612330T= , CM000673.2:g.17612330T=	GRCh38
NC_000011.9:g.17633877T= , CM000673.1:g.17633877T=	GRCh37
NC_000011.8:g.17590453T=	NCBI36
NG_033191.1:g.69958T=
NG_033191.2:g.69958T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6328T=	ENSP00000382323.2:p.Cys2110=
ENST00000399397.6:c.6292T= MANE Select	ENSP00000382329.2:p.Cys2098=
ENST00000342528.2:c.3346T=	ENSP00000341666.2:p.Cys1116=
ENST00000399391.6:c.6328T=	ENSP00000382323.2:p.Cys2110=
ENST00000399397.5:c.6292T=	ENSP00000382329.2:p.Cys2098=
NM_001277269.1:c.6328T=	NP_001264198.1:p.Cys2110=
NM_001292063.1:c.6292T=	NP_001278992.1:p.Cys2098=
NM_001277269.2:c.6328T=	NP_001264198.1:p.Cys2110=
NM_001292063.2:c.6292T= MANE Select	NP_001278992.1:p.Cys2098=