Canonical Allele Identifier: CA2657843622

Gene: ODC1

Linked Data

• gnomAD v4: 2-10447605-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447605A>T , CM000664.2:g.10447605A>T	GRCh38
NC_000002.11:g.10587731A>T , CM000664.1:g.10587731A>T	GRCh37
NC_000002.10:g.10505182A>T	NCBI36
NG_012105.1:g.5723T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-128+23T>A	ENSP00000390691.2:n.-128+23T>A
ENST00000446285.6:c.-128+516T>A	ENSP00000514632.1:n.-128+516T>A
ENST00000699835.1:c.-549T>A	ENSP00000514633.1:n.-549T>A
ENST00000699836.1:c.-18+516T>A	ENSP00000514634.1:n.-18+516T>A
ENST00000234111.9:c.-128+516T>A MANE Select	ENSP00000234111.4:n.-128+516T>A
ENST00000234111.8:c.-128+516T>A	ENSP00000234111.4:n.-128+516T>A
ENST00000405333.5:c.-259T>A	ENSP00000385333.1:n.-259T>A
ENST00000443218.1:c.-128+23T>A	ENSP00000390691.1:n.-128+23T>A
ENST00000446285.5:n.189+516T>A
NM_001287188.1:c.-415+516T>A	NP_001274117.1:n.-415+516T>A
NM_001287189.1:c.-259T>A	NP_001274118.1:n.-259T>A
NM_001287190.1:c.-128+23T>A	NP_001274119.1:n.-128+23T>A
NM_002539.2:c.-128+516T>A	NP_002530.1:n.-128+516T>A
NM_002539.3:c.-128+516T>A MANE Select	NP_002530.1:n.-128+516T>A
NM_001287188.2:c.-415+516T>A	NP_001274117.1:n.-415+516T>A
NM_001287189.2:c.-259T>A	NP_001274118.1:n.-259T>A
NM_001287190.2:c.-128+23T>A	NP_001274119.1:n.-128+23T>A