Canonical Allele Identifier: CA754503007

Gene: ODC1

Linked Data

• dbSNP Id: rs1359038268
• MyVariant Identifiers: chr2:g.10587616_10587617del (hg19) ; chr2:g.10447490_10447491del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447490_10447491del , CM000664.2:g.10447490_10447491del	GRCh38
NC_000002.11:g.10587616_10587617del , CM000664.1:g.10587616_10587617del	GRCh37
NC_000002.10:g.10505067_10505068del	NCBI36
NG_012105.1:g.5837_5838del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-128+137_-128+138del	ENSP00000390691.2:n.-128+137_-128+138del
ENST00000446285.6:c.-128+630_-128+631del	ENSP00000514632.1:n.-128+630_-128+631del
ENST00000699835.1:c.-435_-434del	ENSP00000514633.1:n.-435_-434del
ENST00000699836.1:c.-18+630_-18+631del	ENSP00000514634.1:n.-18+630_-18+631del
ENST00000234111.9:c.-128+630_-128+631del MANE Select	ENSP00000234111.4:n.-128+630_-128+631del
ENST00000234111.8:c.-128+630_-128+631del	ENSP00000234111.4:n.-128+630_-128+631del
ENST00000405333.5:c.-145_-144del	ENSP00000385333.1:n.-145_-144del
ENST00000443218.1:c.-128+137_-128+138del	ENSP00000390691.1:n.-128+137_-128+138del
ENST00000446285.5:n.189+630_189+631del
NM_001287188.1:c.-415+630_-415+631del	NP_001274117.1:n.-415+630_-415+631del
NM_001287189.1:c.-145_-144del	NP_001274118.1:n.-145_-144del
NM_001287190.1:c.-128+137_-128+138del	NP_001274119.1:n.-128+137_-128+138del
NM_002539.2:c.-128+630_-128+631del	NP_002530.1:n.-128+630_-128+631del
NM_002539.3:c.-128+630_-128+631del MANE Select	NP_002530.1:n.-128+630_-128+631del
NM_001287188.2:c.-415+630_-415+631del	NP_001274117.1:n.-415+630_-415+631del
NM_001287189.2:c.-145_-144del	NP_001274118.1:n.-145_-144del
NM_001287190.2:c.-128+137_-128+138del	NP_001274119.1:n.-128+137_-128+138del