Canonical Allele Identifier: CA2514678606

Gene: ODC1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447685T>G , CM000664.2:g.10447685T>G	GRCh38
NC_000002.11:g.10587811T>G , CM000664.1:g.10587811T>G	GRCh37
NC_000002.10:g.10505262T>G	NCBI36
NG_012105.1:g.5643A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-185A>C	ENSP00000390691.2:n.-185A>C
ENST00000446285.6:c.-128+436A>C	ENSP00000514632.1:n.-128+436A>C
ENST00000699835.1:c.-629A>C	ENSP00000514633.1:n.-629A>C
ENST00000699836.1:c.-18+436A>C	ENSP00000514634.1:n.-18+436A>C
ENST00000234111.9:c.-128+436A>C MANE Select	ENSP00000234111.4:n.-128+436A>C
ENST00000234111.8:c.-128+436A>C	ENSP00000234111.4:n.-128+436A>C
ENST00000405333.5:c.-339A>C	ENSP00000385333.1:n.-339A>C
ENST00000443218.1:c.-185A>C	ENSP00000390691.1:n.-185A>C
ENST00000446285.5:n.189+436A>C
NM_001287188.1:c.-415+436A>C	NP_001274117.1:n.-415+436A>C
NM_001287189.1:c.-339A>C	NP_001274118.1:n.-339A>C
NM_001287190.1:c.-185A>C	NP_001274119.1:n.-185A>C
NM_002539.2:c.-128+436A>C	NP_002530.1:n.-128+436A>C
NM_002539.3:c.-128+436A>C MANE Select	NP_002530.1:n.-128+436A>C
NM_001287188.2:c.-415+436A>C	NP_001274117.1:n.-415+436A>C
NM_001287189.2:c.-339A>C	NP_001274118.1:n.-339A>C
NM_001287190.2:c.-185A>C	NP_001274119.1:n.-185A>C