Canonical Allele Identifier: CA379811693
Gene: OTOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.17553466A>G , CM000673.2:g.17553466A>G GRCh38
NC_000011.9:g.17575013A>G , CM000673.1:g.17575013A>G GRCh37
NC_000011.8:g.17531589A>G NCBI36
NG_033191.1:g.11094A>G
NG_033191.2:g.11094A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399391.7:c.523A>G ENSP00000382323.2:p.Ser175Gly
ENST00000399397.6:c.487A>G MANE Select ENSP00000382329.2:p.Ser163Gly
ENST00000399391.6:c.523A>G ENSP00000382323.2:p.Ser175Gly
ENST00000399397.5:c.487A>G ENSP00000382329.2:p.Ser163Gly
ENST00000498332.5:n.393A>G
NM_001277269.1:c.523A>G NP_001264198.1:p.Ser175Gly
NM_001292063.1:c.487A>G NP_001278992.1:p.Ser163Gly
NM_001277269.2:c.523A>G NP_001264198.1:p.Ser175Gly
NM_001292063.2:c.487A>G MANE Select NP_001278992.1:p.Ser163Gly