Canonical Allele Identifier: CA379804229

Gene: OTOG

Linked Data

• gnomAD v4: 11-17612642-C-A
• MyVariant Identifiers: chr11:g.17634189C>A (hg19) ; chr11:g.17612642C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17612642C>A , CM000673.2:g.17612642C>A	GRCh38
NC_000011.9:g.17634189C>A , CM000673.1:g.17634189C>A	GRCh37
NC_000011.8:g.17590765C>A	NCBI36
NG_033191.1:g.70270C>A
NG_033191.2:g.70270C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.6351C>A	ENSP00000382323.2:p.Asp2117Glu
ENST00000399397.6:c.6315C>A MANE Select	ENSP00000382329.2:p.Asp2105Glu
ENST00000342528.2:c.3369C>A	ENSP00000341666.2:p.Asp1123Glu
ENST00000399391.6:c.6351C>A	ENSP00000382323.2:p.Asp2117Glu
ENST00000399397.5:c.6315C>A	ENSP00000382329.2:p.Asp2105Glu
NM_001277269.1:c.6351C>A	NP_001264198.1:p.Asp2117Glu
NM_001292063.1:c.6315C>A	NP_001278992.1:p.Asp2105Glu
NM_001277269.2:c.6351C>A	NP_001264198.1:p.Asp2117Glu
NM_001292063.2:c.6315C>A MANE Select	NP_001278992.1:p.Asp2105Glu