Canonical Allele Identifier: CA409203646
Gene: CD40 HGNC NCBI

Linked Data

ClinVar Variation Id: 632741
ClinVar RCV Id: RCV000780087
dbSNP Id: rs1261429888

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46122290G>A , CM000682.2:g.46122290G>A GRCh38
NC_000020.10:g.44750929G>A , CM000682.1:g.44750929G>A GRCh37
NC_000020.9:g.44184336G>A NCBI36
NG_007279.1:g.9024G>A , LRG_40:g.9024G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.284G>A ENSP00000512095.1:n.284G>A
ENST00000489304.6:c.188G>A ENSP00000512096.1:p.Gly63Asp
ENST00000695669.1:n.261G>A
ENST00000695670.1:n.168G>A
ENST00000695671.1:c.188G>A ENSP00000512093.1:p.Gly63Asp
ENST00000695672.1:n.113G>A
ENST00000695673.1:n.53G>A
ENST00000372285.8:c.188G>A MANE Select ENSP00000361359.3:p.Gly63Asp
ENST00000372276.7:c.188G>A ENSP00000361350.3:p.Gly63Asp
ENST00000372285.7:c.188G>A ENSP00000361359.3:p.Gly63Asp
ENST00000466205.5:c.184G>A
ENST00000477696.5:n.255G>A
ENST00000489304.5:n.181G>A
ENST00000620709.4:c.188G>A ENSP00000484074.1:p.Gly63Asp
NM_001250.5:c.188G>A NP_001241.1:p.Gly63Asp
NM_001302753.1:c.188G>A NP_001289682.1:p.Gly63Asp
NM_152854.3:c.188G>A NP_690593.1:p.Gly63Asp
NR_126502.1:n.278G>A
XM_005260617.2:c.188G>A XP_005260674.1:p.Gly63Asp
XM_005260619.2:c.188G>A XP_005260676.1:p.Gly63Asp
XM_011529109.1:c.188G>A XP_011527411.1:p.Gly63Asp
XR_936660.1:n.282G>A
NM_001322421.1:c.188G>A NP_001309350.1:p.Gly63Asp
NM_001322422.1:c.188G>A NP_001309351.1:p.Gly63Asp
NM_001362758.1:c.188G>A NP_001349687.1:p.Gly63Asp
NR_136327.1:n.278G>A
XM_005260619.3:c.188G>A XP_005260676.1:p.Gly63Asp
XM_011529109.2:c.188G>A XP_011527411.1:p.Gly63Asp
XM_017028135.1:c.188G>A XP_016883624.1:p.Gly63Asp
XM_017028136.1:c.188G>A XP_016883625.1:p.Gly63Asp
NM_001250.6:c.188G>A MANE Select NP_001241.1:p.Gly63Asp
NM_001302753.2:c.188G>A NP_001289682.1:p.Gly63Asp
NM_001322421.2:c.188G>A NP_001309350.1:p.Gly63Asp
NM_001322422.2:c.188G>A NP_001309351.1:p.Gly63Asp
NM_001362758.2:c.188G>A NP_001349687.1:p.Gly63Asp
NM_152854.4:c.188G>A NP_690593.1:p.Gly63Asp
NR_126502.2:n.218G>A
NR_136327.2:n.218G>A