Canonical Allele Identifier: CA2657843844
Gene: ODC1 HGNC NCBI

Linked Data

gnomAD v4: 2-10447812-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447812G>A , CM000664.2:g.10447812G>A GRCh38
NC_000002.11:g.10587938G>A , CM000664.1:g.10587938G>A GRCh37
NC_000002.10:g.10505389G>A NCBI36
NG_012105.1:g.5516C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-312C>T ENSP00000390691.2:n.-312C>T
ENST00000446285.6:c.-128+309C>T ENSP00000514632.1:n.-128+309C>T
ENST00000699835.1:c.-756C>T ENSP00000514633.1:n.-756C>T
ENST00000699836.1:c.-18+309C>T ENSP00000514634.1:n.-18+309C>T
ENST00000234111.9:c.-128+309C>T MANE Select ENSP00000234111.4:n.-128+309C>T
ENST00000234111.8:c.-128+309C>T ENSP00000234111.4:n.-128+309C>T
ENST00000446285.5:n.189+309C>T
NM_001287188.1:c.-415+309C>T NP_001274117.1:n.-415+309C>T
NM_002539.2:c.-128+309C>T NP_002530.1:n.-128+309C>T
NM_002539.3:c.-128+309C>T MANE Select NP_002530.1:n.-128+309C>T
NM_001287188.2:c.-415+309C>T NP_001274117.1:n.-415+309C>T
NM_001287189.2:c.-466C>T NP_001274118.1:n.-466C>T
NM_001287190.2:c.-312C>T NP_001274119.1:n.-312C>T