Canonical Allele Identifier: CA2488522426
Gene: ODC1 HGNC NCBI

Linked Data

dbSNP Id: rs1672074613

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447734G>T , CM000664.2:g.10447734G>T GRCh38
NC_000002.11:g.10587860G>T , CM000664.1:g.10587860G>T GRCh37
NC_000002.10:g.10505311G>T NCBI36
NG_012105.1:g.5594C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-234C>A ENSP00000390691.2:n.-234C>A
ENST00000446285.6:c.-128+387C>A ENSP00000514632.1:n.-128+387C>A
ENST00000699835.1:c.-678C>A ENSP00000514633.1:n.-678C>A
ENST00000699836.1:c.-18+387C>A ENSP00000514634.1:n.-18+387C>A
ENST00000234111.9:c.-128+387C>A MANE Select ENSP00000234111.4:n.-128+387C>A
ENST00000234111.8:c.-128+387C>A ENSP00000234111.4:n.-128+387C>A
ENST00000405333.5:c.-388C>A ENSP00000385333.1:n.-388C>A
ENST00000443218.1:c.-234C>A ENSP00000390691.1:n.-234C>A
ENST00000446285.5:n.189+387C>A
NM_001287188.1:c.-415+387C>A NP_001274117.1:n.-415+387C>A
NM_001287189.1:c.-388C>A NP_001274118.1:n.-388C>A
NM_001287190.1:c.-234C>A NP_001274119.1:n.-234C>A
NM_002539.2:c.-128+387C>A NP_002530.1:n.-128+387C>A
NM_002539.3:c.-128+387C>A MANE Select NP_002530.1:n.-128+387C>A
NM_001287188.2:c.-415+387C>A NP_001274117.1:n.-415+387C>A
NM_001287189.2:c.-388C>A NP_001274118.1:n.-388C>A
NM_001287190.2:c.-234C>A NP_001274119.1:n.-234C>A