Canonical Allele Identifier: CA2657843562

Gene: ODC1

Linked Data

• gnomAD v4: 2-10447514-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447514C>T , CM000664.2:g.10447514C>T	GRCh38
NC_000002.11:g.10587640C>T , CM000664.1:g.10587640C>T	GRCh37
NC_000002.10:g.10505091C>T	NCBI36
NG_012105.1:g.5814G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-128+114G>A	ENSP00000390691.2:n.-128+114G>A
ENST00000446285.6:c.-128+607G>A	ENSP00000514632.1:n.-128+607G>A
ENST00000699835.1:c.-458G>A	ENSP00000514633.1:n.-458G>A
ENST00000699836.1:c.-18+607G>A	ENSP00000514634.1:n.-18+607G>A
ENST00000234111.9:c.-128+607G>A MANE Select	ENSP00000234111.4:n.-128+607G>A
ENST00000234111.8:c.-128+607G>A	ENSP00000234111.4:n.-128+607G>A
ENST00000405333.5:c.-168G>A	ENSP00000385333.1:n.-168G>A
ENST00000443218.1:c.-128+114G>A	ENSP00000390691.1:n.-128+114G>A
ENST00000446285.5:n.189+607G>A
NM_001287188.1:c.-415+607G>A	NP_001274117.1:n.-415+607G>A
NM_001287189.1:c.-168G>A	NP_001274118.1:n.-168G>A
NM_001287190.1:c.-128+114G>A	NP_001274119.1:n.-128+114G>A
NM_002539.2:c.-128+607G>A	NP_002530.1:n.-128+607G>A
NM_002539.3:c.-128+607G>A MANE Select	NP_002530.1:n.-128+607G>A
NM_001287188.2:c.-415+607G>A	NP_001274117.1:n.-415+607G>A
NM_001287189.2:c.-168G>A	NP_001274118.1:n.-168G>A
NM_001287190.2:c.-128+114G>A	NP_001274119.1:n.-128+114G>A