Canonical Allele Identifier: CA530540440

Gene: ODC1

Linked Data

• dbSNP Id: rs1297973079
• gnomAD v2: 2-10587918-G-T
• gnomAD v3: 2-10447792-G-T
• gnomAD v4: 2-10447792-G-T
• MyVariant Identifiers: chr2:g.10587918G>T (hg19) ; chr2:g.10447792G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447792G>T , CM000664.2:g.10447792G>T	GRCh38
NC_000002.11:g.10587918G>T , CM000664.1:g.10587918G>T	GRCh37
NC_000002.10:g.10505369G>T	NCBI36
NG_012105.1:g.5536C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-292C>A	ENSP00000390691.2:n.-292C>A
ENST00000446285.6:c.-128+329C>A	ENSP00000514632.1:n.-128+329C>A
ENST00000699835.1:c.-736C>A	ENSP00000514633.1:n.-736C>A
ENST00000699836.1:c.-18+329C>A	ENSP00000514634.1:n.-18+329C>A
ENST00000234111.9:c.-128+329C>A MANE Select	ENSP00000234111.4:n.-128+329C>A
ENST00000234111.8:c.-128+329C>A	ENSP00000234111.4:n.-128+329C>A
ENST00000446285.5:n.189+329C>A
NM_001287188.1:c.-415+329C>A	NP_001274117.1:n.-415+329C>A
NM_001287189.1:c.-446C>A	NP_001274118.1:n.-446C>A
NM_001287190.1:c.-292C>A	NP_001274119.1:n.-292C>A
NM_002539.2:c.-128+329C>A	NP_002530.1:n.-128+329C>A
NM_002539.3:c.-128+329C>A MANE Select	NP_002530.1:n.-128+329C>A
NM_001287188.2:c.-415+329C>A	NP_001274117.1:n.-415+329C>A
NM_001287189.2:c.-446C>A	NP_001274118.1:n.-446C>A
NM_001287190.2:c.-292C>A	NP_001274119.1:n.-292C>A