Canonical Allele Identifier: CA473310822

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17656446C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17634899C>G , CM000673.2:g.17634899C>G	GRCh38
NC_000011.9:g.17656446C>G , CM000673.1:g.17656446C>G	GRCh37
NC_000011.8:g.17613022C>G	NCBI36
NG_033191.1:g.92527C>G
NG_033191.2:g.92527C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7572C>G	ENSP00000382323.2:p.Arg2524=
ENST00000399397.6:c.7536C>G MANE Select	ENSP00000382329.2:p.Arg2512=
ENST00000342528.2:c.4322-711C>G	ENSP00000341666.2:n.4322-711C>G
ENST00000399391.6:c.7572C>G	ENSP00000382323.2:p.Arg2524=
ENST00000399397.5:c.7536C>G	ENSP00000382329.2:p.Arg2512=
NM_001277269.1:c.7572C>G	NP_001264198.1:p.Arg2524=
NM_001292063.1:c.7536C>G	NP_001278992.1:p.Arg2512=
NM_001277269.2:c.7572C>G	NP_001264198.1:p.Arg2524=
NM_001292063.2:c.7536C>G MANE Select	NP_001278992.1:p.Arg2512=