Canonical Allele Identifier: CA473305613

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17633852C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612305C>A , CM000673.2:g.17612305C>A	GRCh38
NC_000011.9:g.17633852C>A , CM000673.1:g.17633852C>A	GRCh37
NC_000011.8:g.17590428C>A	NCBI36
NG_033191.1:g.69933C>A
NG_033191.2:g.69933C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6303C>A	ENSP00000382323.2:p.Arg2101=
ENST00000399397.6:c.6267C>A MANE Select	ENSP00000382329.2:p.Arg2089=
ENST00000342528.2:c.3321C>A	ENSP00000341666.2:p.Arg1107=
ENST00000399391.6:c.6303C>A	ENSP00000382323.2:p.Arg2101=
ENST00000399397.5:c.6267C>A	ENSP00000382329.2:p.Arg2089=
NM_001277269.1:c.6303C>A	NP_001264198.1:p.Arg2101=
NM_001292063.1:c.6267C>A	NP_001278992.1:p.Arg2089=
NM_001277269.2:c.6303C>A	NP_001264198.1:p.Arg2101=
NM_001292063.2:c.6267C>A MANE Select	NP_001278992.1:p.Arg2089=