Canonical Allele Identifier: CA409212504
Gene: CD40 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46129040A>C , CM000682.2:g.46129040A>C GRCh38
NC_000020.10:g.44757679A>C , CM000682.1:g.44757679A>C GRCh37
NC_000020.9:g.44191086A>C NCBI36
NG_007279.1:g.15774A>C , LRG_40:g.15774A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000489304.6:c.917A>C ENSP00000512096.1:n.917A>C
ENST00000695675.1:n.2710A>C
ENST00000372285.8:c.834A>C MANE Select ENSP00000361359.3:p.Ter278Cys
ENST00000372276.7:c.*160A>C ENSP00000361350.3:n.*160A>C
ENST00000372285.7:c.834A>C ENSP00000361359.3:p.Ter278Cys
ENST00000466205.5:c.736A>C
ENST00000489304.5:n.910A>C
ENST00000620709.4:c.*381A>C ENSP00000484074.1:n.*381A>C
NM_001250.5:c.834A>C NP_001241.1:p.Ter278Cys
NM_001302753.1:c.*160A>C NP_001289682.1:n.*160A>C
NM_152854.3:c.*160A>C NP_690593.1:n.*160A>C
NR_126502.1:n.927A>C
XM_005260617.2:c.846A>C XP_005260674.1:p.Ter282Cys
XM_005260619.2:c.690A>C XP_005260676.1:p.Ter230Cys
XR_936660.1:n.834A>C
NM_001322421.1:c.846A>C NP_001309350.1:p.Ter282Cys
NM_001322422.1:c.678A>C NP_001309351.1:p.Ter226Cys
NM_001362758.1:c.*160A>C NP_001349687.1:n.*160A>C
NR_136327.1:n.830A>C
XM_005260619.3:c.690A>C XP_005260676.1:p.Ter230Cys
XM_017028135.1:c.869A>C XP_016883624.1:p.Glu290Ala
XM_017028136.1:c.767A>C XP_016883625.1:p.Glu256Ala
NM_001250.6:c.834A>C MANE Select NP_001241.1:p.Ter278Cys
NM_001302753.2:c.*160A>C NP_001289682.1:n.*160A>C
NM_001322421.2:c.846A>C NP_001309350.1:p.Ter282Cys
NM_001322422.2:c.678A>C NP_001309351.1:p.Ter226Cys
NM_001362758.2:c.*160A>C NP_001349687.1:n.*160A>C
NM_152854.4:c.*160A>C NP_690593.1:n.*160A>C
NR_126502.2:n.867A>C
NR_136327.2:n.770A>C