Canonical Allele Identifier: CA409205185
Gene: CD40 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46122687A>G , CM000682.2:g.46122687A>G GRCh38
NC_000020.10:g.44751326A>G , CM000682.1:g.44751326A>G GRCh37
NC_000020.9:g.44184733A>G NCBI36
NG_007279.1:g.9421A>G , LRG_40:g.9421A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.430A>G ENSP00000512095.1:n.430A>G
ENST00000489304.6:c.334A>G ENSP00000512096.1:p.Thr112Ala
ENST00000695669.1:n.407A>G
ENST00000695670.1:n.314A>G
ENST00000695671.1:c.334A>G ENSP00000512093.1:p.Thr112Ala
ENST00000695672.1:n.259A>G
ENST00000695673.1:n.199A>G
ENST00000372285.8:c.334A>G MANE Select ENSP00000361359.3:p.Thr112Ala
ENST00000372276.7:c.334A>G ENSP00000361350.3:p.Thr112Ala
ENST00000372285.7:c.334A>G ENSP00000361359.3:p.Thr112Ala
ENST00000461171.1:n.119A>G
ENST00000466205.5:c.330A>G
ENST00000477696.5:n.401A>G
ENST00000489304.5:n.327A>G
ENST00000620709.4:c.334A>G ENSP00000484074.1:p.Thr112Ala
NM_001250.5:c.334A>G NP_001241.1:p.Thr112Ala
NM_001302753.1:c.334A>G NP_001289682.1:p.Thr112Ala
NM_152854.3:c.334A>G NP_690593.1:p.Thr112Ala
NR_126502.1:n.424A>G
XM_005260617.2:c.334A>G XP_005260674.1:p.Thr112Ala
XM_005260619.2:c.334A>G XP_005260676.1:p.Thr112Ala
XM_011529109.1:c.334A>G XP_011527411.1:p.Thr112Ala
XR_936660.1:n.428A>G
NM_001322421.1:c.334A>G NP_001309350.1:p.Thr112Ala
NM_001322422.1:c.334A>G NP_001309351.1:p.Thr112Ala
NM_001362758.1:c.334A>G NP_001349687.1:p.Thr112Ala
NR_136327.1:n.424A>G
XM_005260619.3:c.334A>G XP_005260676.1:p.Thr112Ala
XM_011529109.2:c.334A>G XP_011527411.1:p.Thr112Ala
XM_017028135.1:c.334A>G XP_016883624.1:p.Thr112Ala
XM_017028136.1:c.334A>G XP_016883625.1:p.Thr112Ala
NM_001250.6:c.334A>G MANE Select NP_001241.1:p.Thr112Ala
NM_001302753.2:c.334A>G NP_001289682.1:p.Thr112Ala
NM_001322421.2:c.334A>G NP_001309350.1:p.Thr112Ala
NM_001322422.2:c.334A>G NP_001309351.1:p.Thr112Ala
NM_001362758.2:c.334A>G NP_001349687.1:p.Thr112Ala
NM_152854.4:c.334A>G NP_690593.1:p.Thr112Ala
NR_126502.2:n.364A>G
NR_136327.2:n.364A>G