Canonical Allele Identifier: CA2748840364
Gene: ODC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447511del , CM000664.2:g.10447511del GRCh38
NC_000002.11:g.10587637del , CM000664.1:g.10587637del GRCh37
NC_000002.10:g.10505088del NCBI36
NG_012105.1:g.5818del

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-128+118del ENSP00000390691.2:n.-128+118del
ENST00000446285.6:c.-128+611del ENSP00000514632.1:n.-128+611del
ENST00000699835.1:c.-454del ENSP00000514633.1:n.-454del
ENST00000699836.1:c.-18+611del ENSP00000514634.1:n.-18+611del
ENST00000234111.9:c.-128+611del MANE Select ENSP00000234111.4:n.-128+611del
ENST00000234111.8:c.-128+611del ENSP00000234111.4:n.-128+611del
ENST00000405333.5:c.-164del ENSP00000385333.1:n.-164del
ENST00000443218.1:c.-128+118del ENSP00000390691.1:n.-128+118del
ENST00000446285.5:n.189+611del
NM_001287188.1:c.-415+611del NP_001274117.1:n.-415+611del
NM_001287189.1:c.-164del NP_001274118.1:n.-164del
NM_001287190.1:c.-128+118del NP_001274119.1:n.-128+118del
NM_002539.2:c.-128+611del NP_002530.1:n.-128+611del
NM_002539.3:c.-128+611del MANE Select NP_002530.1:n.-128+611del
NM_001287188.2:c.-415+611del NP_001274117.1:n.-415+611del
NM_001287189.2:c.-164del NP_001274118.1:n.-164del
NM_001287190.2:c.-128+118del NP_001274119.1:n.-128+118del