Canonical Allele Identifier: CA2488522330
Gene: ODC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447570C= , CM000664.2:g.10447570C= GRCh38
NC_000002.11:g.10587696C= , CM000664.1:g.10587696C= GRCh37
NC_000002.10:g.10505147C= NCBI36
NG_012105.1:g.5758G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-128+58G= ENSP00000390691.2:n.-128+58G=
ENST00000446285.6:c.-128+551G= ENSP00000514632.1:n.-128+551G=
ENST00000699835.1:c.-514G= ENSP00000514633.1:n.-514G=
ENST00000699836.1:c.-18+551G= ENSP00000514634.1:n.-18+551G=
ENST00000234111.9:c.-128+551G= MANE Select ENSP00000234111.4:n.-128+551G=
ENST00000234111.8:c.-128+551G= ENSP00000234111.4:n.-128+551G=
ENST00000405333.5:c.-224G= ENSP00000385333.1:n.-224G=
ENST00000443218.1:c.-128+58G= ENSP00000390691.1:n.-128+58G=
ENST00000446285.5:n.189+551G=
NM_001287188.1:c.-415+551G= NP_001274117.1:n.-415+551G=
NM_001287189.1:c.-224G= NP_001274118.1:n.-224G=
NM_001287190.1:c.-128+58G= NP_001274119.1:n.-128+58G=
NM_002539.2:c.-128+551G= NP_002530.1:n.-128+551G=
NM_002539.3:c.-128+551G= MANE Select NP_002530.1:n.-128+551G=
NM_001287188.2:c.-415+551G= NP_001274117.1:n.-415+551G=
NM_001287189.2:c.-224G= NP_001274118.1:n.-224G=
NM_001287190.2:c.-128+58G= NP_001274119.1:n.-128+58G=