Canonical Allele Identifier: CA2488522406
Gene: ODC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447707_10447713delinsAGGCCGG , CM000664.2:g.10447707_10447713delinsAGGCCGG GRCh38
NC_000002.11:g.10587833_10587839delinsAGGCCGG , CM000664.1:g.10587833_10587839delinsAGGCCGG GRCh37
NC_000002.10:g.10505284_10505290delinsAGGCCGG NCBI36
NG_012105.1:g.5615_5621delinsCCGGCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-213_-207delinsCCGGCCT ENSP00000390691.2:n.-213_-207delinsCCGGCCT
ENST00000446285.6:c.-128+408_-128+414delinsCCGGCCT ENSP00000514632.1:n.-128+408_-128+414delinsCCGGCCT
ENST00000699835.1:c.-657_-651delinsCCGGCCT ENSP00000514633.1:n.-657_-651delinsCCGGCCT
ENST00000699836.1:c.-18+408_-18+414delinsCCGGCCT ENSP00000514634.1:n.-18+408_-18+414delinsCCGGCCT
ENST00000234111.9:c.-128+408_-128+414delinsCCGGCCT MANE Select ENSP00000234111.4:n.-128+408_-128+414delinsCCGGCCT
ENST00000234111.8:c.-128+408_-128+414delinsCCGGCCT ENSP00000234111.4:n.-128+408_-128+414delinsCCGGCCT
ENST00000405333.5:c.-367_-361delinsCCGGCCT ENSP00000385333.1:n.-367_-361delinsCCGGCCT
ENST00000443218.1:c.-213_-207delinsCCGGCCT ENSP00000390691.1:n.-213_-207delinsCCGGCCT
ENST00000446285.5:n.189+408_189+414delinsCCGGCCT
NM_001287188.1:c.-415+408_-415+414delinsCCGGCCT NP_001274117.1:n.-415+408_-415+414delinsCCGGCCT
NM_001287189.1:c.-367_-361delinsCCGGCCT NP_001274118.1:n.-367_-361delinsCCGGCCT
NM_001287190.1:c.-213_-207delinsCCGGCCT NP_001274119.1:n.-213_-207delinsCCGGCCT
NM_002539.2:c.-128+408_-128+414delinsCCGGCCT NP_002530.1:n.-128+408_-128+414delinsCCGGCCT
NM_002539.3:c.-128+408_-128+414delinsCCGGCCT MANE Select NP_002530.1:n.-128+408_-128+414delinsCCGGCCT
NM_001287188.2:c.-415+408_-415+414delinsCCGGCCT NP_001274117.1:n.-415+408_-415+414delinsCCGGCCT
NM_001287189.2:c.-367_-361delinsCCGGCCT NP_001274118.1:n.-367_-361delinsCCGGCCT
NM_001287190.2:c.-213_-207delinsCCGGCCT NP_001274119.1:n.-213_-207delinsCCGGCCT