Canonical Allele Identifier: CA2366529047
Gene: CD40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118343T>G , CM000682.2:g.46118343T>G GRCh38
NC_000020.10:g.44746982T>G , CM000682.1:g.44746982T>G GRCh37
NC_000020.9:g.44180389T>G NCBI36
NG_007279.1:g.5077T>G , LRG_40:g.5077T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695669.1:n.73T>G
ENST00000695670.1:n.59T>G
ENST00000695671.1:c.-1T>G ENSP00000512093.1:n.-1T>G
ENST00000695672.1:n.4T>G
ENST00000372285.8:c.-1T>G MANE Select ENSP00000361359.3:n.-1T>G
ENST00000372276.7:c.-1T>G ENSP00000361350.3:n.-1T>G
ENST00000372285.7:c.-1T>G ENSP00000361359.3:n.-1T>G
ENST00000620709.4:c.-1T>G ENSP00000484074.1:n.-1T>G
NM_001250.5:c.-1T>G NP_001241.1:n.-1T>G
NM_001302753.1:c.-1T>G NP_001289682.1:n.-1T>G
NM_152854.3:c.-1T>G NP_690593.1:n.-1T>G
NR_126502.1:n.90T>G
XM_005260617.2:c.-1T>G XP_005260674.1:n.-1T>G
XM_005260619.2:c.-1T>G XP_005260676.1:n.-1T>G
XM_011529109.1:c.-1T>G XP_011527411.1:n.-1T>G
XR_936660.1:n.94T>G
NM_001322421.1:c.-1T>G NP_001309350.1:n.-1T>G
NM_001322422.1:c.-1T>G NP_001309351.1:n.-1T>G
NM_001362758.1:c.-1T>G NP_001349687.1:n.-1T>G
NR_136327.1:n.90T>G
XM_005260619.3:c.-1T>G XP_005260676.1:n.-1T>G
XM_011529109.2:c.-1T>G XP_011527411.1:n.-1T>G
XM_017028135.1:c.-1T>G XP_016883624.1:n.-1T>G
XM_017028136.1:c.-1T>G XP_016883625.1:n.-1T>G
NM_001250.6:c.-1T>G MANE Select NP_001241.1:n.-1T>G
NM_001302753.2:c.-1T>G NP_001289682.1:n.-1T>G
NM_001322421.2:c.-1T>G NP_001309350.1:n.-1T>G
NM_001322422.2:c.-1T>G NP_001309351.1:n.-1T>G
NM_001362758.2:c.-1T>G NP_001349687.1:n.-1T>G
NM_152854.4:c.-1T>G NP_690593.1:n.-1T>G
NR_126502.2:n.30T>G
NR_136327.2:n.30T>G