Canonical Allele Identifier: CA2577414827
Gene: CD40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118271A>C , CM000682.2:g.46118271A>C GRCh38
NC_000020.10:g.44746910A>C , CM000682.1:g.44746910A>C GRCh37
NC_000020.9:g.44180317A>C NCBI36
NG_007279.1:g.5005A>C , LRG_40:g.5005A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695669.1:n.1A>C
NM_001250.5:c.-73A>C NP_001241.1:n.-73A>C
NM_001302753.1:c.-73A>C NP_001289682.1:n.-73A>C
NM_152854.3:c.-73A>C NP_690593.1:n.-73A>C
NR_126502.1:n.18A>C
XM_005260617.2:c.-73A>C XP_005260674.1:n.-73A>C
XM_005260619.2:c.-73A>C XP_005260676.1:n.-73A>C
XM_011529109.1:c.-73A>C XP_011527411.1:n.-73A>C
XR_936660.1:n.22A>C
NM_001322421.1:c.-73A>C NP_001309350.1:n.-73A>C
NM_001322422.1:c.-73A>C NP_001309351.1:n.-73A>C
NM_001362758.1:c.-73A>C NP_001349687.1:n.-73A>C
NR_136327.1:n.18A>C
XM_005260619.3:c.-73A>C XP_005260676.1:n.-73A>C
XM_011529109.2:c.-73A>C XP_011527411.1:n.-73A>C
XM_017028135.1:c.-73A>C XP_016883624.1:n.-73A>C
XM_017028136.1:c.-73A>C XP_016883625.1:n.-73A>C