Canonical Allele Identifier: CA2488522302
Gene: ODC1 HGNC NCBI

Linked Data

dbSNP Id: rs1672064697

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447507T>G , CM000664.2:g.10447507T>G GRCh38
NC_000002.11:g.10587633T>G , CM000664.1:g.10587633T>G GRCh37
NC_000002.10:g.10505084T>G NCBI36
NG_012105.1:g.5821A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-128+121A>C ENSP00000390691.2:n.-128+121A>C
ENST00000446285.6:c.-128+614A>C ENSP00000514632.1:n.-128+614A>C
ENST00000699835.1:c.-451A>C ENSP00000514633.1:n.-451A>C
ENST00000699836.1:c.-18+614A>C ENSP00000514634.1:n.-18+614A>C
ENST00000234111.9:c.-128+614A>C MANE Select ENSP00000234111.4:n.-128+614A>C
ENST00000234111.8:c.-128+614A>C ENSP00000234111.4:n.-128+614A>C
ENST00000405333.5:c.-161A>C ENSP00000385333.1:n.-161A>C
ENST00000443218.1:c.-128+121A>C ENSP00000390691.1:n.-128+121A>C
ENST00000446285.5:n.189+614A>C
NM_001287188.1:c.-415+614A>C NP_001274117.1:n.-415+614A>C
NM_001287189.1:c.-161A>C NP_001274118.1:n.-161A>C
NM_001287190.1:c.-128+121A>C NP_001274119.1:n.-128+121A>C
NM_002539.2:c.-128+614A>C NP_002530.1:n.-128+614A>C
NM_002539.3:c.-128+614A>C MANE Select NP_002530.1:n.-128+614A>C
NM_001287188.2:c.-415+614A>C NP_001274117.1:n.-415+614A>C
NM_001287189.2:c.-161A>C NP_001274118.1:n.-161A>C
NM_001287190.2:c.-128+121A>C NP_001274119.1:n.-128+121A>C