Canonical Allele Identifier: CA2488522522
Gene: ODC1 HGNC NCBI

Linked Data

dbSNP Id: rs1672083322

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447853G>A , CM000664.2:g.10447853G>A GRCh38
NC_000002.11:g.10587979G>A , CM000664.1:g.10587979G>A GRCh37
NC_000002.10:g.10505430G>A NCBI36
NG_012105.1:g.5475C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-353C>T ENSP00000390691.2:n.-353C>T
ENST00000446285.6:c.-128+268C>T ENSP00000514632.1:n.-128+268C>T
ENST00000699835.1:c.-797C>T ENSP00000514633.1:n.-797C>T
ENST00000699836.1:c.-18+268C>T ENSP00000514634.1:n.-18+268C>T
ENST00000234111.9:c.-128+268C>T MANE Select ENSP00000234111.4:n.-128+268C>T
ENST00000234111.8:c.-128+268C>T ENSP00000234111.4:n.-128+268C>T
ENST00000446285.5:n.189+268C>T
NM_001287188.1:c.-415+268C>T NP_001274117.1:n.-415+268C>T
NM_002539.2:c.-128+268C>T NP_002530.1:n.-128+268C>T
NM_002539.3:c.-128+268C>T MANE Select NP_002530.1:n.-128+268C>T
NM_001287188.2:c.-415+268C>T NP_001274117.1:n.-415+268C>T
NM_001287189.2:c.-507C>T NP_001274118.1:n.-507C>T
NM_001287190.2:c.-353C>T NP_001274119.1:n.-353C>T