Canonical Allele Identifier: CA2839538559
Gene: CD40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118295_46118296del , CM000682.2:g.46118295_46118296del GRCh38
NC_000020.10:g.44746934_44746935del , CM000682.1:g.44746934_44746935del GRCh37
NC_000020.9:g.44180341_44180342del NCBI36
NG_007279.1:g.5029_5030del , LRG_40:g.5029_5030del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695669.1:n.25_26del
ENST00000695670.1:n.11_12del
ENST00000372285.7:c.-49_-48del ENSP00000361359.3:n.-49_-48del
ENST00000620709.4:c.-49_-48del ENSP00000484074.1:n.-49_-48del
NM_001250.5:c.-49_-48del NP_001241.1:n.-49_-48del
NM_001302753.1:c.-49_-48del NP_001289682.1:n.-49_-48del
NM_152854.3:c.-49_-48del NP_690593.1:n.-49_-48del
NR_126502.1:n.42_43del
XM_005260617.2:c.-49_-48del XP_005260674.1:n.-49_-48del
XM_005260619.2:c.-49_-48del XP_005260676.1:n.-49_-48del
XM_011529109.1:c.-49_-48del XP_011527411.1:n.-49_-48del
XR_936660.1:n.46_47del
NM_001322421.1:c.-49_-48del NP_001309350.1:n.-49_-48del
NM_001322422.1:c.-49_-48del NP_001309351.1:n.-49_-48del
NM_001362758.1:c.-49_-48del NP_001349687.1:n.-49_-48del
NR_136327.1:n.42_43del
XM_005260619.3:c.-49_-48del XP_005260676.1:n.-49_-48del
XM_011529109.2:c.-49_-48del XP_011527411.1:n.-49_-48del
XM_017028135.1:c.-49_-48del XP_016883624.1:n.-49_-48del
XM_017028136.1:c.-49_-48del XP_016883625.1:n.-49_-48del