Canonical Allele Identifier: CA2488522317
Gene: ODC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447541_10447543delinsTCA , CM000664.2:g.10447541_10447543delinsTCA GRCh38
NC_000002.11:g.10587667_10587669delinsTCA , CM000664.1:g.10587667_10587669delinsTCA GRCh37
NC_000002.10:g.10505118_10505120delinsTCA NCBI36
NG_012105.1:g.5785_5787delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-128+85_-128+87delinsTGA ENSP00000390691.2:n.-128+85_-128+87delinsTGA
ENST00000446285.6:c.-128+578_-128+580delinsTGA ENSP00000514632.1:n.-128+578_-128+580delinsTGA
ENST00000699835.1:c.-487_-485delinsTGA ENSP00000514633.1:n.-487_-485delinsTGA
ENST00000699836.1:c.-18+578_-18+580delinsTGA ENSP00000514634.1:n.-18+578_-18+580delinsTGA
ENST00000234111.9:c.-128+578_-128+580delinsTGA MANE Select ENSP00000234111.4:n.-128+578_-128+580delinsTGA
ENST00000234111.8:c.-128+578_-128+580delinsTGA ENSP00000234111.4:n.-128+578_-128+580delinsTGA
ENST00000405333.5:c.-197_-195delinsTGA ENSP00000385333.1:n.-197_-195delinsTGA
ENST00000443218.1:c.-128+85_-128+87delinsTGA ENSP00000390691.1:n.-128+85_-128+87delinsTGA
ENST00000446285.5:n.189+578_189+580delinsTGA
NM_001287188.1:c.-415+578_-415+580delinsTGA NP_001274117.1:n.-415+578_-415+580delinsTGA
NM_001287189.1:c.-197_-195delinsTGA NP_001274118.1:n.-197_-195delinsTGA
NM_001287190.1:c.-128+85_-128+87delinsTGA NP_001274119.1:n.-128+85_-128+87delinsTGA
NM_002539.2:c.-128+578_-128+580delinsTGA NP_002530.1:n.-128+578_-128+580delinsTGA
NM_002539.3:c.-128+578_-128+580delinsTGA MANE Select NP_002530.1:n.-128+578_-128+580delinsTGA
NM_001287188.2:c.-415+578_-415+580delinsTGA NP_001274117.1:n.-415+578_-415+580delinsTGA
NM_001287189.2:c.-197_-195delinsTGA NP_001274118.1:n.-197_-195delinsTGA
NM_001287190.2:c.-128+85_-128+87delinsTGA NP_001274119.1:n.-128+85_-128+87delinsTGA