Canonical Allele Identifier: CA935545386

Gene: OTOG

Linked Data

• dbSNP Id: rs1854239565
• gnomAD v3: 11-17635352-G-A
• gnomAD v4: 11-17635352-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635352G>A , CM000673.2:g.17635352G>A	GRCh38
NC_000011.9:g.17656899G>A , CM000673.1:g.17656899G>A	GRCh37
NC_000011.8:g.17613475G>A	NCBI36
NG_033191.1:g.92980G>A
NG_033191.2:g.92980G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7729+165G>A	ENSP00000382323.2:n.7729+165G>A
ENST00000399397.6:c.7693+165G>A MANE Select	ENSP00000382329.2:n.7693+165G>A
ENST00000342528.2:c.4322-258G>A	ENSP00000341666.2:n.4322-258G>A
ENST00000399391.6:c.7729+165G>A	ENSP00000382323.2:n.7729+165G>A
ENST00000399397.5:c.7693+165G>A	ENSP00000382329.2:n.7693+165G>A
NM_001277269.1:c.7729+165G>A	NP_001264198.1:n.7729+165G>A
NM_001292063.1:c.7693+165G>A	NP_001278992.1:n.7693+165G>A
NM_001277269.2:c.7729+165G>A	NP_001264198.1:n.7729+165G>A
NM_001292063.2:c.7693+165G>A MANE Select	NP_001278992.1:n.7693+165G>A