Canonical Allele Identifier: CA2488522290

Gene: ODC1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447489_10447491delinsCCT , CM000664.2:g.10447489_10447491delinsCCT	GRCh38
NC_000002.11:g.10587615_10587617delinsCCT , CM000664.1:g.10587615_10587617delinsCCT	GRCh37
NC_000002.10:g.10505066_10505068delinsCCT	NCBI36
NG_012105.1:g.5837_5839delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-128+137_-128+139delinsAGG	ENSP00000390691.2:n.-128+137_-128+139delinsAGG
ENST00000446285.6:c.-128+630_-128+632delinsAGG	ENSP00000514632.1:n.-128+630_-128+632delinsAGG
ENST00000699835.1:c.-435_-433delinsAGG	ENSP00000514633.1:n.-435_-433delinsAGG
ENST00000699836.1:c.-18+630_-18+632delinsAGG	ENSP00000514634.1:n.-18+630_-18+632delinsAGG
ENST00000234111.9:c.-128+630_-128+632delinsAGG MANE Select	ENSP00000234111.4:n.-128+630_-128+632delinsAGG
ENST00000234111.8:c.-128+630_-128+632delinsAGG	ENSP00000234111.4:n.-128+630_-128+632delinsAGG
ENST00000405333.5:c.-145_-143delinsAGG	ENSP00000385333.1:n.-145_-143delinsAGG
ENST00000443218.1:c.-128+137_-128+139delinsAGG	ENSP00000390691.1:n.-128+137_-128+139delinsAGG
ENST00000446285.5:n.189+630_189+632delinsAGG
NM_001287188.1:c.-415+630_-415+632delinsAGG	NP_001274117.1:n.-415+630_-415+632delinsAGG
NM_001287189.1:c.-145_-143delinsAGG	NP_001274118.1:n.-145_-143delinsAGG
NM_001287190.1:c.-128+137_-128+139delinsAGG	NP_001274119.1:n.-128+137_-128+139delinsAGG
NM_002539.2:c.-128+630_-128+632delinsAGG	NP_002530.1:n.-128+630_-128+632delinsAGG
NM_002539.3:c.-128+630_-128+632delinsAGG MANE Select	NP_002530.1:n.-128+630_-128+632delinsAGG
NM_001287188.2:c.-415+630_-415+632delinsAGG	NP_001274117.1:n.-415+630_-415+632delinsAGG
NM_001287189.2:c.-145_-143delinsAGG	NP_001274118.1:n.-145_-143delinsAGG
NM_001287190.2:c.-128+137_-128+139delinsAGG	NP_001274119.1:n.-128+137_-128+139delinsAGG