Canonical Allele Identifier: CA379810606

Gene: OTOG

Linked Data

• MyVariant Identifiers: chr11:g.17574699T>A (hg19) ; chr11:g.17553152T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.17553152T>A , CM000673.2:g.17553152T>A	GRCh38
NC_000011.9:g.17574699T>A , CM000673.1:g.17574699T>A	GRCh37
NC_000011.8:g.17531275T>A	NCBI36
NG_033191.1:g.10780T>A
NG_033191.2:g.10780T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399391.7:c.362T>A	ENSP00000382323.2:p.Val121Glu
ENST00000399397.6:c.326T>A MANE Select	ENSP00000382329.2:p.Val109Glu
ENST00000399391.6:c.362T>A	ENSP00000382323.2:p.Val121Glu
ENST00000399397.5:c.326T>A	ENSP00000382329.2:p.Val109Glu
ENST00000428619.1:c.143T>A	ENSP00000399057.2:p.Val48Glu
ENST00000498332.5:n.232T>A
NM_001277269.1:c.362T>A	NP_001264198.1:p.Val121Glu
NM_001292063.1:c.326T>A	NP_001278992.1:p.Val109Glu
NM_001277269.2:c.362T>A	NP_001264198.1:p.Val121Glu
NM_001292063.2:c.326T>A MANE Select	NP_001278992.1:p.Val109Glu