Canonical Allele Identifier: CA1027506337
Gene: ODC1 HGNC NCBI

Linked Data

dbSNP Id: rs1672066040

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447544_10447545del , CM000664.2:g.10447544_10447545del GRCh38
NC_000002.11:g.10587670_10587671del , CM000664.1:g.10587670_10587671del GRCh37
NC_000002.10:g.10505121_10505122del NCBI36
NG_012105.1:g.5785_5786del

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-128+85_-128+86del ENSP00000390691.2:n.-128+85_-128+86del
ENST00000446285.6:c.-128+578_-128+579del ENSP00000514632.1:n.-128+578_-128+579del
ENST00000699835.1:c.-487_-486del ENSP00000514633.1:n.-487_-486del
ENST00000699836.1:c.-18+578_-18+579del ENSP00000514634.1:n.-18+578_-18+579del
ENST00000234111.9:c.-128+578_-128+579del MANE Select ENSP00000234111.4:n.-128+578_-128+579del
ENST00000234111.8:c.-128+578_-128+579del ENSP00000234111.4:n.-128+578_-128+579del
ENST00000405333.5:c.-197_-196del ENSP00000385333.1:n.-197_-196del
ENST00000443218.1:c.-128+85_-128+86del ENSP00000390691.1:n.-128+85_-128+86del
ENST00000446285.5:n.189+578_189+579del
NM_001287188.1:c.-415+578_-415+579del NP_001274117.1:n.-415+578_-415+579del
NM_001287189.1:c.-197_-196del NP_001274118.1:n.-197_-196del
NM_001287190.1:c.-128+85_-128+86del NP_001274119.1:n.-128+85_-128+86del
NM_002539.2:c.-128+578_-128+579del NP_002530.1:n.-128+578_-128+579del
NM_002539.3:c.-128+578_-128+579del MANE Select NP_002530.1:n.-128+578_-128+579del
NM_001287188.2:c.-415+578_-415+579del NP_001274117.1:n.-415+578_-415+579del
NM_001287189.2:c.-197_-196del NP_001274118.1:n.-197_-196del
NM_001287190.2:c.-128+85_-128+86del NP_001274119.1:n.-128+85_-128+86del