Canonical Allele Identifier: CA2488522519
Gene: ODC1 HGNC NCBI

Linked Data

dbSNP Id: rs1572149759

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447852G>C , CM000664.2:g.10447852G>C GRCh38
NC_000002.11:g.10587978G>C , CM000664.1:g.10587978G>C GRCh37
NC_000002.10:g.10505429G>C NCBI36
NG_012105.1:g.5476C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-352C>G ENSP00000390691.2:n.-352C>G
ENST00000446285.6:c.-128+269C>G ENSP00000514632.1:n.-128+269C>G
ENST00000699835.1:c.-796C>G ENSP00000514633.1:n.-796C>G
ENST00000699836.1:c.-18+269C>G ENSP00000514634.1:n.-18+269C>G
ENST00000234111.9:c.-128+269C>G MANE Select ENSP00000234111.4:n.-128+269C>G
ENST00000234111.8:c.-128+269C>G ENSP00000234111.4:n.-128+269C>G
ENST00000446285.5:n.189+269C>G
NM_001287188.1:c.-415+269C>G NP_001274117.1:n.-415+269C>G
NM_002539.2:c.-128+269C>G NP_002530.1:n.-128+269C>G
NM_002539.3:c.-128+269C>G MANE Select NP_002530.1:n.-128+269C>G
NM_001287188.2:c.-415+269C>G NP_001274117.1:n.-415+269C>G
NM_001287189.2:c.-506C>G NP_001274118.1:n.-506C>G
NM_001287190.2:c.-352C>G NP_001274119.1:n.-352C>G