Canonical Allele Identifier: CA379797509

Gene: OTOG

Linked Data

• gnomAD v4: 11-17610356-C-A
• MyVariant Identifiers: chr11:g.17631903C>A (hg19) ; chr11:g.17610356C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17610356C>A , CM000673.2:g.17610356C>A	GRCh38
NC_000011.9:g.17631903C>A , CM000673.1:g.17631903C>A	GRCh37
NC_000011.8:g.17588479C>A	NCBI36
NG_033191.1:g.67984C>A
NG_033191.2:g.67984C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000399391.7:c.5092C>A	ENSP00000382323.2:p.Gln1698Lys
ENST00000399397.6:c.5056C>A MANE Select	ENSP00000382329.2:p.Gln1686Lys
ENST00000342528.2:c.2110C>A	ENSP00000341666.2:p.Gln704Lys
ENST00000399391.6:c.5092C>A	ENSP00000382323.2:p.Gln1698Lys
ENST00000399397.5:c.5056C>A	ENSP00000382329.2:p.Gln1686Lys
NM_001277269.1:c.5092C>A	NP_001264198.1:p.Gln1698Lys
NM_001292063.1:c.5056C>A	NP_001278992.1:p.Gln1686Lys
NM_001277269.2:c.5092C>A	NP_001264198.1:p.Gln1698Lys
NM_001292063.2:c.5056C>A MANE Select	NP_001278992.1:p.Gln1686Lys