Canonical Allele Identifier: CA42456919
Gene: ODC1 HGNC NCBI

Linked Data

dbSNP Id: rs941099674
gnomAD v2: 2-10588050-G-A
gnomAD v3: 2-10447924-G-A
gnomAD v4: 2-10447924-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447924G>A , CM000664.2:g.10447924G>A GRCh38
NC_000002.11:g.10588050G>A , CM000664.1:g.10588050G>A GRCh37
NC_000002.10:g.10505501G>A NCBI36
NG_012105.1:g.5404C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000443218.2:c.-424C>T ENSP00000390691.2:n.-424C>T
ENST00000446285.6:c.-128+197C>T ENSP00000514632.1:n.-128+197C>T
ENST00000699835.1:c.-868C>T ENSP00000514633.1:n.-868C>T
ENST00000699836.1:c.-18+197C>T ENSP00000514634.1:n.-18+197C>T
ENST00000234111.9:c.-128+197C>T MANE Select ENSP00000234111.4:n.-128+197C>T
ENST00000234111.8:c.-128+197C>T ENSP00000234111.4:n.-128+197C>T
ENST00000446285.5:n.189+197C>T
NM_001287188.1:c.-415+197C>T NP_001274117.1:n.-415+197C>T
NM_002539.2:c.-128+197C>T NP_002530.1:n.-128+197C>T
NM_002539.3:c.-128+197C>T MANE Select NP_002530.1:n.-128+197C>T
NM_001287188.2:c.-415+197C>T NP_001274117.1:n.-415+197C>T
NM_001287189.2:c.-578C>T NP_001274118.1:n.-578C>T
NM_001287190.2:c.-424C>T NP_001274119.1:n.-424C>T