Canonical Allele Identifier: CA2488522328
Gene: ODC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447562C= , CM000664.2:g.10447562C= GRCh38
NC_000002.11:g.10587688C= , CM000664.1:g.10587688C= GRCh37
NC_000002.10:g.10505139C= NCBI36
NG_012105.1:g.5766G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-128+66G= ENSP00000390691.2:n.-128+66G=
ENST00000446285.6:c.-128+559G= ENSP00000514632.1:n.-128+559G=
ENST00000699835.1:c.-506G= ENSP00000514633.1:n.-506G=
ENST00000699836.1:c.-18+559G= ENSP00000514634.1:n.-18+559G=
ENST00000234111.9:c.-128+559G= MANE Select ENSP00000234111.4:n.-128+559G=
ENST00000234111.8:c.-128+559G= ENSP00000234111.4:n.-128+559G=
ENST00000405333.5:c.-216G= ENSP00000385333.1:n.-216G=
ENST00000443218.1:c.-128+66G= ENSP00000390691.1:n.-128+66G=
ENST00000446285.5:n.189+559G=
NM_001287188.1:c.-415+559G= NP_001274117.1:n.-415+559G=
NM_001287189.1:c.-216G= NP_001274118.1:n.-216G=
NM_001287190.1:c.-128+66G= NP_001274119.1:n.-128+66G=
NM_002539.2:c.-128+559G= NP_002530.1:n.-128+559G=
NM_002539.3:c.-128+559G= MANE Select NP_002530.1:n.-128+559G=
NM_001287188.2:c.-415+559G= NP_001274117.1:n.-415+559G=
NM_001287189.2:c.-216G= NP_001274118.1:n.-216G=
NM_001287190.2:c.-128+66G= NP_001274119.1:n.-128+66G=