Canonical Allele Identifier: CA2488522392

Gene: ODC1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.10447680A= , CM000664.2:g.10447680A=	GRCh38
NC_000002.11:g.10587806A= , CM000664.1:g.10587806A=	GRCh37
NC_000002.10:g.10505257A=	NCBI36
NG_012105.1:g.5648T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000443218.2:c.-180T=	ENSP00000390691.2:n.-180T=
ENST00000446285.6:c.-128+441T=	ENSP00000514632.1:n.-128+441T=
ENST00000699835.1:c.-624T=	ENSP00000514633.1:n.-624T=
ENST00000699836.1:c.-18+441T=	ENSP00000514634.1:n.-18+441T=
ENST00000234111.9:c.-128+441T= MANE Select	ENSP00000234111.4:n.-128+441T=
ENST00000234111.8:c.-128+441T=	ENSP00000234111.4:n.-128+441T=
ENST00000405333.5:c.-334T=	ENSP00000385333.1:n.-334T=
ENST00000443218.1:c.-180T=	ENSP00000390691.1:n.-180T=
ENST00000446285.5:n.189+441T=
NM_001287188.1:c.-415+441T=	NP_001274117.1:n.-415+441T=
NM_001287189.1:c.-334T=	NP_001274118.1:n.-334T=
NM_001287190.1:c.-180T=	NP_001274119.1:n.-180T=
NM_002539.2:c.-128+441T=	NP_002530.1:n.-128+441T=
NM_002539.3:c.-128+441T= MANE Select	NP_002530.1:n.-128+441T=
NM_001287188.2:c.-415+441T=	NP_001274117.1:n.-415+441T=
NM_001287189.2:c.-334T=	NP_001274118.1:n.-334T=
NM_001287190.2:c.-180T=	NP_001274119.1:n.-180T=