Canonical Allele Identifier: CA42456898

Gene: ODC1

Linked Data

• dbSNP Id: rs115030661
• gnomAD v2: 2-10588045-C-A
• gnomAD v3: 2-10447919-C-A
• gnomAD v4: 2-10447919-C-A
• MyVariant Identifiers: chr2:g.10588045C>A (hg19) ; chr2:g.10447919C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447919C>A , CM000664.2:g.10447919C>A	GRCh38
NC_000002.11:g.10588045C>A , CM000664.1:g.10588045C>A	GRCh37
NC_000002.10:g.10505496C>A	NCBI36
NG_012105.1:g.5409G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000443218.2:c.-419G>T	ENSP00000390691.2:n.-419G>T
ENST00000446285.6:c.-128+202G>T	ENSP00000514632.1:n.-128+202G>T
ENST00000699835.1:c.-863G>T	ENSP00000514633.1:n.-863G>T
ENST00000699836.1:c.-18+202G>T	ENSP00000514634.1:n.-18+202G>T
ENST00000234111.9:c.-128+202G>T MANE Select	ENSP00000234111.4:n.-128+202G>T
ENST00000234111.8:c.-128+202G>T	ENSP00000234111.4:n.-128+202G>T
ENST00000446285.5:n.189+202G>T
NM_001287188.1:c.-415+202G>T	NP_001274117.1:n.-415+202G>T
NM_002539.2:c.-128+202G>T	NP_002530.1:n.-128+202G>T
NM_002539.3:c.-128+202G>T MANE Select	NP_002530.1:n.-128+202G>T
NM_001287188.2:c.-415+202G>T	NP_001274117.1:n.-415+202G>T
NM_001287189.2:c.-573G>T	NP_001274118.1:n.-573G>T
NM_001287190.2:c.-419G>T	NP_001274119.1:n.-419G>T