Canonical Allele Identifier: CA754503143

Gene: ODC1

Linked Data

• dbSNP Id: rs1443970852
• MyVariant Identifiers: chr2:g.10587834_10587839del (hg19) ; chr2:g.10447708_10447713del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447712_10447717del , CM000664.2:g.10447712_10447717del	GRCh38
NC_000002.11:g.10587838_10587843del , CM000664.1:g.10587838_10587843del	GRCh37
NC_000002.10:g.10505289_10505294del	NCBI36
NG_012105.1:g.5615_5620del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-213_-208del	ENSP00000390691.2:n.-213_-208del
ENST00000446285.6:c.-128+408_-128+413del	ENSP00000514632.1:n.-128+408_-128+413del
ENST00000699835.1:c.-657_-652del	ENSP00000514633.1:n.-657_-652del
ENST00000699836.1:c.-18+408_-18+413del	ENSP00000514634.1:n.-18+408_-18+413del
ENST00000234111.9:c.-128+408_-128+413del MANE Select	ENSP00000234111.4:n.-128+408_-128+413del
ENST00000234111.8:c.-128+408_-128+413del	ENSP00000234111.4:n.-128+408_-128+413del
ENST00000405333.5:c.-367_-362del	ENSP00000385333.1:n.-367_-362del
ENST00000443218.1:c.-213_-208del	ENSP00000390691.1:n.-213_-208del
ENST00000446285.5:n.189+408_189+413del
NM_001287188.1:c.-415+408_-415+413del	NP_001274117.1:n.-415+408_-415+413del
NM_001287189.1:c.-367_-362del	NP_001274118.1:n.-367_-362del
NM_001287190.1:c.-213_-208del	NP_001274119.1:n.-213_-208del
NM_002539.2:c.-128+408_-128+413del	NP_002530.1:n.-128+408_-128+413del
NM_002539.3:c.-128+408_-128+413del MANE Select	NP_002530.1:n.-128+408_-128+413del
NM_001287188.2:c.-415+408_-415+413del	NP_001274117.1:n.-415+408_-415+413del
NM_001287189.2:c.-367_-362del	NP_001274118.1:n.-367_-362del
NM_001287190.2:c.-213_-208del	NP_001274119.1:n.-213_-208del