Canonical Allele Identifier: CA2657843818

Gene: ODC1

Linked Data

• gnomAD v4: 2-10447784-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447788del , CM000664.2:g.10447788del	GRCh38
NC_000002.11:g.10587914del , CM000664.1:g.10587914del	GRCh37
NC_000002.10:g.10505365del	NCBI36
NG_012105.1:g.5543del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-285del	ENSP00000390691.2:n.-285del
ENST00000446285.6:c.-128+336del	ENSP00000514632.1:n.-128+336del
ENST00000699835.1:c.-729del	ENSP00000514633.1:n.-729del
ENST00000699836.1:c.-18+336del	ENSP00000514634.1:n.-18+336del
ENST00000234111.9:c.-128+336del MANE Select	ENSP00000234111.4:n.-128+336del
ENST00000234111.8:c.-128+336del	ENSP00000234111.4:n.-128+336del
ENST00000443218.1:c.-285del	ENSP00000390691.1:n.-285del
ENST00000446285.5:n.189+336del
NM_001287188.1:c.-415+336del	NP_001274117.1:n.-415+336del
NM_001287189.1:c.-439del	NP_001274118.1:n.-439del
NM_001287190.1:c.-285del	NP_001274119.1:n.-285del
NM_002539.2:c.-128+336del	NP_002530.1:n.-128+336del
NM_002539.3:c.-128+336del MANE Select	NP_002530.1:n.-128+336del
NM_001287188.2:c.-415+336del	NP_001274117.1:n.-415+336del
NM_001287189.2:c.-439del	NP_001274118.1:n.-439del
NM_001287190.2:c.-285del	NP_001274119.1:n.-285del