Canonical Allele Identifier: CA1027506342
Gene: ODC1 HGNC NCBI

Linked Data

dbSNP Id: rs1672066693
gnomAD v3: 2-10447557-A-C
gnomAD v4: 2-10447557-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447557A>C , CM000664.2:g.10447557A>C GRCh38
NC_000002.11:g.10587683A>C , CM000664.1:g.10587683A>C GRCh37
NC_000002.10:g.10505134A>C NCBI36
NG_012105.1:g.5771T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-128+71T>G ENSP00000390691.2:n.-128+71T>G
ENST00000446285.6:c.-128+564T>G ENSP00000514632.1:n.-128+564T>G
ENST00000699835.1:c.-501T>G ENSP00000514633.1:n.-501T>G
ENST00000699836.1:c.-18+564T>G ENSP00000514634.1:n.-18+564T>G
ENST00000234111.9:c.-128+564T>G MANE Select ENSP00000234111.4:n.-128+564T>G
ENST00000234111.8:c.-128+564T>G ENSP00000234111.4:n.-128+564T>G
ENST00000405333.5:c.-211T>G ENSP00000385333.1:n.-211T>G
ENST00000443218.1:c.-128+71T>G ENSP00000390691.1:n.-128+71T>G
ENST00000446285.5:n.189+564T>G
NM_001287188.1:c.-415+564T>G NP_001274117.1:n.-415+564T>G
NM_001287189.1:c.-211T>G NP_001274118.1:n.-211T>G
NM_001287190.1:c.-128+71T>G NP_001274119.1:n.-128+71T>G
NM_002539.2:c.-128+564T>G NP_002530.1:n.-128+564T>G
NM_002539.3:c.-128+564T>G MANE Select NP_002530.1:n.-128+564T>G
NM_001287188.2:c.-415+564T>G NP_001274117.1:n.-415+564T>G
NM_001287189.2:c.-211T>G NP_001274118.1:n.-211T>G
NM_001287190.2:c.-128+71T>G NP_001274119.1:n.-128+71T>G