Canonical Allele Identifier: CA2737036810
Gene: CD40 HGNC NCBI

Linked Data

dbSNP Id: rs2145617068

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46129213A>G , CM000682.2:g.46129213A>G GRCh38
NC_000020.10:g.44757852A>G , CM000682.1:g.44757852A>G GRCh37
NC_000020.9:g.44191259A>G NCBI36
NG_007279.1:g.15947A>G , LRG_40:g.15947A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000489304.6:c.1090A>G ENSP00000512096.1:n.1090A>G
ENST00000695675.1:n.2883A>G
ENST00000372285.8:c.*173A>G MANE Select ENSP00000361359.3:n.*173A>G
ENST00000372276.7:c.*333A>G ENSP00000361350.3:n.*333A>G
ENST00000372285.7:c.*173A>G ENSP00000361359.3:n.*173A>G
ENST00000489304.5:n.1083A>G
ENST00000620709.4:c.*554A>G ENSP00000484074.1:n.*554A>G
NM_001250.5:c.*173A>G NP_001241.1:n.*173A>G
NM_001302753.1:c.*333A>G NP_001289682.1:n.*333A>G
NM_152854.3:c.*333A>G NP_690593.1:n.*333A>G
NR_126502.1:n.1100A>G
XM_005260617.2:c.*173A>G XP_005260674.1:n.*173A>G
XM_005260619.2:c.*173A>G XP_005260676.1:n.*173A>G
NM_001322421.1:c.*173A>G NP_001309350.1:n.*173A>G
NM_001322422.1:c.*173A>G NP_001309351.1:n.*173A>G
NM_001362758.1:c.*333A>G NP_001349687.1:n.*333A>G
NR_136327.1:n.1003A>G
XM_005260619.3:c.*173A>G XP_005260676.1:n.*173A>G
XM_017028135.1:c.*70A>G XP_016883624.1:n.*70A>G
XM_017028136.1:c.*70A>G XP_016883625.1:n.*70A>G
NM_001250.6:c.*173A>G MANE Select NP_001241.1:n.*173A>G
NM_001302753.2:c.*333A>G NP_001289682.1:n.*333A>G
NM_001322421.2:c.*173A>G NP_001309350.1:n.*173A>G
NM_001322422.2:c.*173A>G NP_001309351.1:n.*173A>G
NM_001362758.2:c.*333A>G NP_001349687.1:n.*333A>G
NM_152854.4:c.*333A>G NP_690593.1:n.*333A>G
NR_126502.2:n.1040A>G
NR_136327.2:n.943A>G