Canonical Allele Identifier: CA9888513
Gene: CD40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46126737G>C , CM000682.2:g.46126737G>C GRCh38
NC_000020.10:g.44755376G>C , CM000682.1:g.44755376G>C GRCh37
NC_000020.9:g.44188783G>C NCBI36
NG_007279.1:g.13471G>C , LRG_40:g.13471G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.561+36G>C ENSP00000512095.1:n.561+36G>C
ENST00000489304.6:c.559+36G>C ENSP00000512096.1:n.559+36G>C
ENST00000695670.1:n.445+36G>C
ENST00000695671.1:c.595G>C ENSP00000512093.1:p.Gly199Arg
ENST00000695672.1:n.484+36G>C
ENST00000695674.1:n.1038+36G>C
ENST00000695675.1:n.1035G>C
ENST00000372285.8:c.559+36G>C MANE Select ENSP00000361359.3:n.559+36G>C
ENST00000372276.7:c.498-1401G>C ENSP00000361350.3:n.498-1401G>C
ENST00000372285.7:c.559+36G>C ENSP00000361359.3:n.559+36G>C
ENST00000461171.1:n.286G>C
ENST00000466205.5:c.461+36G>C
ENST00000477696.5:n.532+36G>C
ENST00000489304.5:n.552+36G>C
ENST00000620709.4:c.404-1242G>C ENSP00000484074.1:n.404-1242G>C
NM_001250.5:c.559+36G>C NP_001241.1:n.559+36G>C
NM_001302753.1:c.595G>C NP_001289682.1:p.Gly199Arg
NM_152854.3:c.498-1401G>C NP_690593.1:n.498-1401G>C
NR_126502.1:n.494-1242G>C
XM_005260617.2:c.559+36G>C XP_005260674.1:n.559+36G>C
XM_005260619.2:c.404-1401G>C XP_005260676.1:n.404-1401G>C
XM_011529109.1:c.501G>C XP_011527411.1:p.Ter167Tyr
XR_936660.1:n.559+36G>C
NM_001322421.1:c.559+36G>C NP_001309350.1:n.559+36G>C
NM_001322422.1:c.404-1401G>C NP_001309351.1:n.404-1401G>C
NM_001362758.1:c.559+36G>C NP_001349687.1:n.559+36G>C
NR_136327.1:n.555+36G>C
XM_005260619.3:c.404-1401G>C XP_005260676.1:n.404-1401G>C
XM_011529109.2:c.501G>C XP_011527411.1:p.Ter167Tyr
XM_017028135.1:c.595G>C XP_016883624.1:p.Gly199Arg
XM_017028136.1:c.498-1401G>C XP_016883625.1:n.498-1401G>C
NM_001250.6:c.559+36G>C MANE Select NP_001241.1:n.559+36G>C
NM_001302753.2:c.595G>C NP_001289682.1:p.Gly199Arg
NM_001322421.2:c.559+36G>C NP_001309350.1:n.559+36G>C
NM_001322422.2:c.404-1401G>C NP_001309351.1:n.404-1401G>C
NM_001362758.2:c.559+36G>C NP_001349687.1:n.559+36G>C
NM_152854.4:c.498-1401G>C NP_690593.1:n.498-1401G>C
NR_126502.2:n.434-1242G>C
NR_136327.2:n.495+36G>C