Canonical Allele Identifier: CA379811799
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553488A>C , CM000673.2:g.17553488A>C GRCh38
NC_000011.9:g.17575035A>C , CM000673.1:g.17575035A>C GRCh37
NC_000011.8:g.17531611A>C NCBI36
NG_033191.1:g.11116A>C
NG_033191.2:g.11116A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.545A>C ENSP00000382323.2:p.His182Pro
ENST00000399397.6:c.509A>C MANE Select ENSP00000382329.2:p.His170Pro
ENST00000399391.6:c.545A>C ENSP00000382323.2:p.His182Pro
ENST00000399397.5:c.509A>C ENSP00000382329.2:p.His170Pro
ENST00000498332.5:n.415A>C
NM_001277269.1:c.545A>C NP_001264198.1:p.His182Pro
NM_001292063.1:c.509A>C NP_001278992.1:p.His170Pro
NM_001277269.2:c.545A>C NP_001264198.1:p.His182Pro
NM_001292063.2:c.509A>C MANE Select NP_001278992.1:p.His170Pro