Canonical Allele Identifier: CA379813127

Gene: OTOG

Linked Data

• gnomAD v4: 11-17635186-C-A
• MyVariant Identifiers: chr11:g.17656733C>A (hg19) ; chr11:g.17635186C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17635186C>A , CM000673.2:g.17635186C>A	GRCh38
NC_000011.9:g.17656733C>A , CM000673.1:g.17656733C>A	GRCh37
NC_000011.8:g.17613309C>A	NCBI36
NG_033191.1:g.92814C>A
NG_033191.2:g.92814C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.7728C>A	ENSP00000382323.2:p.Cys2576Ter
ENST00000399397.6:c.7692C>A MANE Select	ENSP00000382329.2:p.Cys2564Ter
ENST00000342528.2:c.4322-424C>A	ENSP00000341666.2:n.4322-424C>A
ENST00000399391.6:c.7728C>A	ENSP00000382323.2:p.Cys2576Ter
ENST00000399397.5:c.7692C>A	ENSP00000382329.2:p.Cys2564Ter
NM_001277269.1:c.7728C>A	NP_001264198.1:p.Cys2576Ter
NM_001292063.1:c.7692C>A	NP_001278992.1:p.Cys2564Ter
NM_001277269.2:c.7728C>A	NP_001264198.1:p.Cys2576Ter
NM_001292063.2:c.7692C>A MANE Select	NP_001278992.1:p.Cys2564Ter