Canonical Allele Identifier: CA2748840367

Gene: ODC1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447551T>A , CM000664.2:g.10447551T>A	GRCh38
NC_000002.11:g.10587677T>A , CM000664.1:g.10587677T>A	GRCh37
NC_000002.10:g.10505128T>A	NCBI36
NG_012105.1:g.5777A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-128+77A>T	ENSP00000390691.2:n.-128+77A>T
ENST00000446285.6:c.-128+570A>T	ENSP00000514632.1:n.-128+570A>T
ENST00000699835.1:c.-495A>T	ENSP00000514633.1:n.-495A>T
ENST00000699836.1:c.-18+570A>T	ENSP00000514634.1:n.-18+570A>T
ENST00000234111.9:c.-128+570A>T MANE Select	ENSP00000234111.4:n.-128+570A>T
ENST00000234111.8:c.-128+570A>T	ENSP00000234111.4:n.-128+570A>T
ENST00000405333.5:c.-205A>T	ENSP00000385333.1:n.-205A>T
ENST00000443218.1:c.-128+77A>T	ENSP00000390691.1:n.-128+77A>T
ENST00000446285.5:n.189+570A>T
NM_001287188.1:c.-415+570A>T	NP_001274117.1:n.-415+570A>T
NM_001287189.1:c.-205A>T	NP_001274118.1:n.-205A>T
NM_001287190.1:c.-128+77A>T	NP_001274119.1:n.-128+77A>T
NM_002539.2:c.-128+570A>T	NP_002530.1:n.-128+570A>T
NM_002539.3:c.-128+570A>T MANE Select	NP_002530.1:n.-128+570A>T
NM_001287188.2:c.-415+570A>T	NP_001274117.1:n.-415+570A>T
NM_001287189.2:c.-205A>T	NP_001274118.1:n.-205A>T
NM_001287190.2:c.-128+77A>T	NP_001274119.1:n.-128+77A>T