Canonical Allele Identifier: CA379810922
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553193G>A , CM000673.2:g.17553193G>A GRCh38
NC_000011.9:g.17574740G>A , CM000673.1:g.17574740G>A GRCh37
NC_000011.8:g.17531316G>A NCBI36
NG_033191.1:g.10821G>A
NG_033191.2:g.10821G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.403G>A ENSP00000382323.2:p.Gly135Arg
ENST00000399397.6:c.367G>A MANE Select ENSP00000382329.2:p.Gly123Arg
ENST00000399391.6:c.403G>A ENSP00000382323.2:p.Gly135Arg
ENST00000399397.5:c.367G>A ENSP00000382329.2:p.Gly123Arg
ENST00000428619.1:c.184G>A ENSP00000399057.2:p.Gly62Arg
ENST00000498332.5:n.273G>A
NM_001277269.1:c.403G>A NP_001264198.1:p.Gly135Arg
NM_001292063.1:c.367G>A NP_001278992.1:p.Gly123Arg
NM_001277269.2:c.403G>A NP_001264198.1:p.Gly135Arg
NM_001292063.2:c.367G>A MANE Select NP_001278992.1:p.Gly123Arg