Canonical Allele Identifier: CA473310930

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17656697C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635150C>G , CM000673.2:g.17635150C>G	GRCh38
NC_000011.9:g.17656697C>G , CM000673.1:g.17656697C>G	GRCh37
NC_000011.8:g.17613273C>G	NCBI36
NG_033191.1:g.92778C>G
NG_033191.2:g.92778C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7692C>G	ENSP00000382323.2:p.Gly2564=
ENST00000399397.6:c.7656C>G MANE Select	ENSP00000382329.2:p.Gly2552=
ENST00000342528.2:c.4322-460C>G	ENSP00000341666.2:n.4322-460C>G
ENST00000399391.6:c.7692C>G	ENSP00000382323.2:p.Gly2564=
ENST00000399397.5:c.7656C>G	ENSP00000382329.2:p.Gly2552=
NM_001277269.1:c.7692C>G	NP_001264198.1:p.Gly2564=
NM_001292063.1:c.7656C>G	NP_001278992.1:p.Gly2552=
NM_001277269.2:c.7692C>G	NP_001264198.1:p.Gly2564=
NM_001292063.2:c.7656C>G MANE Select	NP_001278992.1:p.Gly2552=