Canonical Allele Identifier: CA1027506352
Gene: ODC1 HGNC NCBI

Linked Data

dbSNP Id: rs1672067868
gnomAD v3: 2-10447575-C-T
gnomAD v4: 2-10447575-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447575C>T , CM000664.2:g.10447575C>T GRCh38
NC_000002.11:g.10587701C>T , CM000664.1:g.10587701C>T GRCh37
NC_000002.10:g.10505152C>T NCBI36
NG_012105.1:g.5753G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-128+53G>A ENSP00000390691.2:n.-128+53G>A
ENST00000446285.6:c.-128+546G>A ENSP00000514632.1:n.-128+546G>A
ENST00000699835.1:c.-519G>A ENSP00000514633.1:n.-519G>A
ENST00000699836.1:c.-18+546G>A ENSP00000514634.1:n.-18+546G>A
ENST00000234111.9:c.-128+546G>A MANE Select ENSP00000234111.4:n.-128+546G>A
ENST00000234111.8:c.-128+546G>A ENSP00000234111.4:n.-128+546G>A
ENST00000405333.5:c.-229G>A ENSP00000385333.1:n.-229G>A
ENST00000443218.1:c.-128+53G>A ENSP00000390691.1:n.-128+53G>A
ENST00000446285.5:n.189+546G>A
NM_001287188.1:c.-415+546G>A NP_001274117.1:n.-415+546G>A
NM_001287189.1:c.-229G>A NP_001274118.1:n.-229G>A
NM_001287190.1:c.-128+53G>A NP_001274119.1:n.-128+53G>A
NM_002539.2:c.-128+546G>A NP_002530.1:n.-128+546G>A
NM_002539.3:c.-128+546G>A MANE Select NP_002530.1:n.-128+546G>A
NM_001287188.2:c.-415+546G>A NP_001274117.1:n.-415+546G>A
NM_001287189.2:c.-229G>A NP_001274118.1:n.-229G>A
NM_001287190.2:c.-128+53G>A NP_001274119.1:n.-128+53G>A