Canonical Allele Identifier: CA754503261

Gene: ODC1

Linked Data

• dbSNP Id: rs1485852786
• gnomAD v3: 2-10447843-G-T
• gnomAD v4: 2-10447843-G-T
• MyVariant Identifiers: chr2:g.10587969G>T (hg19) ; chr2:g.10447843G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447843G>T , CM000664.2:g.10447843G>T	GRCh38
NC_000002.11:g.10587969G>T , CM000664.1:g.10587969G>T	GRCh37
NC_000002.10:g.10505420G>T	NCBI36
NG_012105.1:g.5485C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-343C>A	ENSP00000390691.2:n.-343C>A
ENST00000446285.6:c.-128+278C>A	ENSP00000514632.1:n.-128+278C>A
ENST00000699835.1:c.-787C>A	ENSP00000514633.1:n.-787C>A
ENST00000699836.1:c.-18+278C>A	ENSP00000514634.1:n.-18+278C>A
ENST00000234111.9:c.-128+278C>A MANE Select	ENSP00000234111.4:n.-128+278C>A
ENST00000234111.8:c.-128+278C>A	ENSP00000234111.4:n.-128+278C>A
ENST00000446285.5:n.189+278C>A
NM_001287188.1:c.-415+278C>A	NP_001274117.1:n.-415+278C>A
NM_002539.2:c.-128+278C>A	NP_002530.1:n.-128+278C>A
NM_002539.3:c.-128+278C>A MANE Select	NP_002530.1:n.-128+278C>A
NM_001287188.2:c.-415+278C>A	NP_001274117.1:n.-415+278C>A
NM_001287189.2:c.-497C>A	NP_001274118.1:n.-497C>A
NM_001287190.2:c.-343C>A	NP_001274119.1:n.-343C>A