Canonical Allele Identifier: CA2657843914

Gene: ODC1

Linked Data

• gnomAD v4: 2-10447923-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447923C>A , CM000664.2:g.10447923C>A	GRCh38
NC_000002.11:g.10588049C>A , CM000664.1:g.10588049C>A	GRCh37
NC_000002.10:g.10505500C>A	NCBI36
NG_012105.1:g.5405G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000443218.2:c.-423G>T	ENSP00000390691.2:n.-423G>T
ENST00000446285.6:c.-128+198G>T	ENSP00000514632.1:n.-128+198G>T
ENST00000699835.1:c.-867G>T	ENSP00000514633.1:n.-867G>T
ENST00000699836.1:c.-18+198G>T	ENSP00000514634.1:n.-18+198G>T
ENST00000234111.9:c.-128+198G>T MANE Select	ENSP00000234111.4:n.-128+198G>T
ENST00000234111.8:c.-128+198G>T	ENSP00000234111.4:n.-128+198G>T
ENST00000446285.5:n.189+198G>T
NM_001287188.1:c.-415+198G>T	NP_001274117.1:n.-415+198G>T
NM_002539.2:c.-128+198G>T	NP_002530.1:n.-128+198G>T
NM_002539.3:c.-128+198G>T MANE Select	NP_002530.1:n.-128+198G>T
NM_001287188.2:c.-415+198G>T	NP_001274117.1:n.-415+198G>T
NM_001287189.2:c.-577G>T	NP_001274118.1:n.-577G>T
NM_001287190.2:c.-423G>T	NP_001274119.1:n.-423G>T