Canonical Allele Identifier: CA379811102
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553382G>C , CM000673.2:g.17553382G>C GRCh38
NC_000011.9:g.17574929G>C , CM000673.1:g.17574929G>C GRCh37
NC_000011.8:g.17531505G>C NCBI36
NG_033191.1:g.11010G>C
NG_033191.2:g.11010G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.439G>C ENSP00000382323.2:p.Glu147Gln
ENST00000399397.6:c.403G>C MANE Select ENSP00000382329.2:p.Glu135Gln
ENST00000399391.6:c.439G>C ENSP00000382323.2:p.Glu147Gln
ENST00000399397.5:c.403G>C ENSP00000382329.2:p.Glu135Gln
ENST00000428619.1:c.220G>C ENSP00000399057.2:p.Glu74Gln
ENST00000498332.5:n.309G>C
NM_001277269.1:c.439G>C NP_001264198.1:p.Glu147Gln
NM_001292063.1:c.403G>C NP_001278992.1:p.Glu135Gln
NM_001277269.2:c.439G>C NP_001264198.1:p.Glu147Gln
NM_001292063.2:c.403G>C MANE Select NP_001278992.1:p.Glu135Gln