Canonical Allele Identifier: CA2612690411

Gene: OTOG

Linked Data

• gnomAD v4: 11-17635315-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635315A>G , CM000673.2:g.17635315A>G	GRCh38
NC_000011.9:g.17656862A>G , CM000673.1:g.17656862A>G	GRCh37
NC_000011.8:g.17613438A>G	NCBI36
NG_033191.1:g.92943A>G
NG_033191.2:g.92943A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7729+128A>G	ENSP00000382323.2:n.7729+128A>G
ENST00000399397.6:c.7693+128A>G MANE Select	ENSP00000382329.2:n.7693+128A>G
ENST00000342528.2:c.4322-295A>G	ENSP00000341666.2:n.4322-295A>G
ENST00000399391.6:c.7729+128A>G	ENSP00000382323.2:n.7729+128A>G
ENST00000399397.5:c.7693+128A>G	ENSP00000382329.2:n.7693+128A>G
NM_001277269.1:c.7729+128A>G	NP_001264198.1:n.7729+128A>G
NM_001292063.1:c.7693+128A>G	NP_001278992.1:n.7693+128A>G
NM_001277269.2:c.7729+128A>G	NP_001264198.1:n.7729+128A>G
NM_001292063.2:c.7693+128A>G MANE Select	NP_001278992.1:n.7693+128A>G