Canonical Allele Identifier: CA2488522439
Gene: ODC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.10447746C= , CM000664.2:g.10447746C= GRCh38
NC_000002.11:g.10587872C= , CM000664.1:g.10587872C= GRCh37
NC_000002.10:g.10505323C= NCBI36
NG_012105.1:g.5582G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000443218.2:c.-246G= ENSP00000390691.2:n.-246G=
ENST00000446285.6:c.-128+375G= ENSP00000514632.1:n.-128+375G=
ENST00000699835.1:c.-690G= ENSP00000514633.1:n.-690G=
ENST00000699836.1:c.-18+375G= ENSP00000514634.1:n.-18+375G=
ENST00000234111.9:c.-128+375G= MANE Select ENSP00000234111.4:n.-128+375G=
ENST00000234111.8:c.-128+375G= ENSP00000234111.4:n.-128+375G=
ENST00000405333.5:c.-400G= ENSP00000385333.1:n.-400G=
ENST00000443218.1:c.-246G= ENSP00000390691.1:n.-246G=
ENST00000446285.5:n.189+375G=
NM_001287188.1:c.-415+375G= NP_001274117.1:n.-415+375G=
NM_001287189.1:c.-400G= NP_001274118.1:n.-400G=
NM_001287190.1:c.-246G= NP_001274119.1:n.-246G=
NM_002539.2:c.-128+375G= NP_002530.1:n.-128+375G=
NM_002539.3:c.-128+375G= MANE Select NP_002530.1:n.-128+375G=
NM_001287188.2:c.-415+375G= NP_001274117.1:n.-415+375G=
NM_001287189.2:c.-400G= NP_001274118.1:n.-400G=
NM_001287190.2:c.-246G= NP_001274119.1:n.-246G=