Canonical Allele Identifier: CA2739725407
Gene: CD40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46129123A>T , CM000682.2:g.46129123A>T GRCh38
NC_000020.10:g.44757762A>T , CM000682.1:g.44757762A>T GRCh37
NC_000020.9:g.44191169A>T NCBI36
NG_007279.1:g.15857A>T , LRG_40:g.15857A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000489304.6:c.1000A>T ENSP00000512096.1:n.1000A>T
ENST00000695675.1:n.2793A>T
ENST00000372285.8:c.*83A>T MANE Select ENSP00000361359.3:n.*83A>T
ENST00000372276.7:c.*243A>T ENSP00000361350.3:n.*243A>T
ENST00000372285.7:c.*83A>T ENSP00000361359.3:n.*83A>T
ENST00000466205.5:c.819A>T
ENST00000489304.5:n.993A>T
ENST00000620709.4:c.*464A>T ENSP00000484074.1:n.*464A>T
NM_001250.5:c.*83A>T NP_001241.1:n.*83A>T
NM_001302753.1:c.*243A>T NP_001289682.1:n.*243A>T
NM_152854.3:c.*243A>T NP_690593.1:n.*243A>T
NR_126502.1:n.1010A>T
XM_005260617.2:c.*83A>T XP_005260674.1:n.*83A>T
XM_005260619.2:c.*83A>T XP_005260676.1:n.*83A>T
NM_001322421.1:c.*83A>T NP_001309350.1:n.*83A>T
NM_001322422.1:c.*83A>T NP_001309351.1:n.*83A>T
NM_001362758.1:c.*243A>T NP_001349687.1:n.*243A>T
NR_136327.1:n.913A>T
XM_005260619.3:c.*83A>T XP_005260676.1:n.*83A>T
XM_017028135.1:c.952A>T XP_016883624.1:p.Arg318Trp
XM_017028136.1:c.850A>T XP_016883625.1:p.Arg284Trp
NM_001250.6:c.*83A>T MANE Select NP_001241.1:n.*83A>T
NM_001302753.2:c.*243A>T NP_001289682.1:n.*243A>T
NM_001322421.2:c.*83A>T NP_001309350.1:n.*83A>T
NM_001322422.2:c.*83A>T NP_001309351.1:n.*83A>T
NM_001362758.2:c.*243A>T NP_001349687.1:n.*243A>T
NM_152854.4:c.*243A>T NP_690593.1:n.*243A>T
NR_126502.2:n.950A>T
NR_136327.2:n.853A>T