Canonical Allele Identifier: CA2657843717
Gene: ODC1 HGNC NCBI

Linked Data

gnomAD v4: 2-10447720-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447720C>A , CM000664.2:g.10447720C>A GRCh38
NC_000002.11:g.10587846C>A , CM000664.1:g.10587846C>A GRCh37
NC_000002.10:g.10505297C>A NCBI36
NG_012105.1:g.5608G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-220G>T ENSP00000390691.2:n.-220G>T
ENST00000446285.6:c.-128+401G>T ENSP00000514632.1:n.-128+401G>T
ENST00000699835.1:c.-664G>T ENSP00000514633.1:n.-664G>T
ENST00000699836.1:c.-18+401G>T ENSP00000514634.1:n.-18+401G>T
ENST00000234111.9:c.-128+401G>T MANE Select ENSP00000234111.4:n.-128+401G>T
ENST00000234111.8:c.-128+401G>T ENSP00000234111.4:n.-128+401G>T
ENST00000405333.5:c.-374G>T ENSP00000385333.1:n.-374G>T
ENST00000443218.1:c.-220G>T ENSP00000390691.1:n.-220G>T
ENST00000446285.5:n.189+401G>T
NM_001287188.1:c.-415+401G>T NP_001274117.1:n.-415+401G>T
NM_001287189.1:c.-374G>T NP_001274118.1:n.-374G>T
NM_001287190.1:c.-220G>T NP_001274119.1:n.-220G>T
NM_002539.2:c.-128+401G>T NP_002530.1:n.-128+401G>T
NM_002539.3:c.-128+401G>T MANE Select NP_002530.1:n.-128+401G>T
NM_001287188.2:c.-415+401G>T NP_001274117.1:n.-415+401G>T
NM_001287189.2:c.-374G>T NP_001274118.1:n.-374G>T
NM_001287190.2:c.-220G>T NP_001274119.1:n.-220G>T