Canonical Allele Identifier: CA379811267

Gene: OTOG

Linked Data

• gnomAD v4: 11-17553399-C-A
• MyVariant Identifiers: chr11:g.17574946C>A (hg19) ; chr11:g.17553399C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553399C>A , CM000673.2:g.17553399C>A	GRCh38
NC_000011.9:g.17574946C>A , CM000673.1:g.17574946C>A	GRCh37
NC_000011.8:g.17531522C>A	NCBI36
NG_033191.1:g.11027C>A
NG_033191.2:g.11027C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.456C>A	ENSP00000382323.2:p.Cys152Ter
ENST00000399397.6:c.420C>A MANE Select	ENSP00000382329.2:p.Cys140Ter
ENST00000399391.6:c.456C>A	ENSP00000382323.2:p.Cys152Ter
ENST00000399397.5:c.420C>A	ENSP00000382329.2:p.Cys140Ter
ENST00000428619.1:c.237C>A	ENSP00000399057.2:p.Cys79Ter
ENST00000498332.5:n.326C>A
NM_001277269.1:c.456C>A	NP_001264198.1:p.Cys152Ter
NM_001292063.1:c.420C>A	NP_001278992.1:p.Cys140Ter
NM_001277269.2:c.456C>A	NP_001264198.1:p.Cys152Ter
NM_001292063.2:c.420C>A MANE Select	NP_001278992.1:p.Cys140Ter