Canonical Allele Identifier: CA409205120
Gene: CD40 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46122682A>C , CM000682.2:g.46122682A>C GRCh38
NC_000020.10:g.44751321A>C , CM000682.1:g.44751321A>C GRCh37
NC_000020.9:g.44184728A>C NCBI36
NG_007279.1:g.9416A>C , LRG_40:g.9416A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.425A>C ENSP00000512095.1:n.425A>C
ENST00000489304.6:c.329A>C ENSP00000512096.1:p.His110Pro
ENST00000695669.1:n.402A>C
ENST00000695670.1:n.309A>C
ENST00000695671.1:c.329A>C ENSP00000512093.1:p.His110Pro
ENST00000695672.1:n.254A>C
ENST00000695673.1:n.194A>C
ENST00000372285.8:c.329A>C MANE Select ENSP00000361359.3:p.His110Pro
ENST00000372276.7:c.329A>C ENSP00000361350.3:p.His110Pro
ENST00000372285.7:c.329A>C ENSP00000361359.3:p.His110Pro
ENST00000461171.1:n.114A>C
ENST00000466205.5:c.325A>C
ENST00000477696.5:n.396A>C
ENST00000489304.5:n.322A>C
ENST00000620709.4:c.329A>C ENSP00000484074.1:p.His110Pro
NM_001250.5:c.329A>C NP_001241.1:p.His110Pro
NM_001302753.1:c.329A>C NP_001289682.1:p.His110Pro
NM_152854.3:c.329A>C NP_690593.1:p.His110Pro
NR_126502.1:n.419A>C
XM_005260617.2:c.329A>C XP_005260674.1:p.His110Pro
XM_005260619.2:c.329A>C XP_005260676.1:p.His110Pro
XM_011529109.1:c.329A>C XP_011527411.1:p.His110Pro
XR_936660.1:n.423A>C
NM_001322421.1:c.329A>C NP_001309350.1:p.His110Pro
NM_001322422.1:c.329A>C NP_001309351.1:p.His110Pro
NM_001362758.1:c.329A>C NP_001349687.1:p.His110Pro
NR_136327.1:n.419A>C
XM_005260619.3:c.329A>C XP_005260676.1:p.His110Pro
XM_011529109.2:c.329A>C XP_011527411.1:p.His110Pro
XM_017028135.1:c.329A>C XP_016883624.1:p.His110Pro
XM_017028136.1:c.329A>C XP_016883625.1:p.His110Pro
NM_001250.6:c.329A>C MANE Select NP_001241.1:p.His110Pro
NM_001302753.2:c.329A>C NP_001289682.1:p.His110Pro
NM_001322421.2:c.329A>C NP_001309350.1:p.His110Pro
NM_001322422.2:c.329A>C NP_001309351.1:p.His110Pro
NM_001362758.2:c.329A>C NP_001349687.1:p.His110Pro
NM_152854.4:c.329A>C NP_690593.1:p.His110Pro
NR_126502.2:n.359A>C
NR_136327.2:n.359A>C