Canonical Allele Identifier: CA754503305

Gene: ODC1

Linked Data

• dbSNP Id: rs1458689448
• gnomAD v4: 2-10447887-C-A
• MyVariant Identifiers: chr2:g.10588013C>A (hg19) ; chr2:g.10447887C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447887C>A , CM000664.2:g.10447887C>A	GRCh38
NC_000002.11:g.10588013C>A , CM000664.1:g.10588013C>A	GRCh37
NC_000002.10:g.10505464C>A	NCBI36
NG_012105.1:g.5441G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-387G>T	ENSP00000390691.2:n.-387G>T
ENST00000446285.6:c.-128+234G>T	ENSP00000514632.1:n.-128+234G>T
ENST00000699835.1:c.-831G>T	ENSP00000514633.1:n.-831G>T
ENST00000699836.1:c.-18+234G>T	ENSP00000514634.1:n.-18+234G>T
ENST00000234111.9:c.-128+234G>T MANE Select	ENSP00000234111.4:n.-128+234G>T
ENST00000234111.8:c.-128+234G>T	ENSP00000234111.4:n.-128+234G>T
ENST00000446285.5:n.189+234G>T
NM_001287188.1:c.-415+234G>T	NP_001274117.1:n.-415+234G>T
NM_002539.2:c.-128+234G>T	NP_002530.1:n.-128+234G>T
NM_002539.3:c.-128+234G>T MANE Select	NP_002530.1:n.-128+234G>T
NM_001287188.2:c.-415+234G>T	NP_001274117.1:n.-415+234G>T
NM_001287189.2:c.-541G>T	NP_001274118.1:n.-541G>T
NM_001287190.2:c.-387G>T	NP_001274119.1:n.-387G>T