Canonical Allele Identifier: CA379811188
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553391A>G , CM000673.2:g.17553391A>G GRCh38
NC_000011.9:g.17574938A>G , CM000673.1:g.17574938A>G GRCh37
NC_000011.8:g.17531514A>G NCBI36
NG_033191.1:g.11019A>G
NG_033191.2:g.11019A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000399391.7:c.448A>G ENSP00000382323.2:p.Ser150Gly
ENST00000399397.6:c.412A>G MANE Select ENSP00000382329.2:p.Ser138Gly
ENST00000399391.6:c.448A>G ENSP00000382323.2:p.Ser150Gly
ENST00000399397.5:c.412A>G ENSP00000382329.2:p.Ser138Gly
ENST00000428619.1:c.229A>G ENSP00000399057.2:p.Ser77Gly
ENST00000498332.5:n.318A>G
NM_001277269.1:c.448A>G NP_001264198.1:p.Ser150Gly
NM_001292063.1:c.412A>G NP_001278992.1:p.Ser138Gly
NM_001277269.2:c.448A>G NP_001264198.1:p.Ser150Gly
NM_001292063.2:c.412A>G MANE Select NP_001278992.1:p.Ser138Gly