Canonical Allele Identifier: CA2366533236
Gene: CD40 HGNC NCBI

Linked Data

dbSNP Id: rs1326510001

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46129124G>A , CM000682.2:g.46129124G>A GRCh38
NC_000020.10:g.44757763G>A , CM000682.1:g.44757763G>A GRCh37
NC_000020.9:g.44191170G>A NCBI36
NG_007279.1:g.15858G>A , LRG_40:g.15858G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000489304.6:c.1001G>A ENSP00000512096.1:n.1001G>A
ENST00000695675.1:n.2794G>A
ENST00000372285.8:c.*84G>A MANE Select ENSP00000361359.3:n.*84G>A
ENST00000372276.7:c.*244G>A ENSP00000361350.3:n.*244G>A
ENST00000372285.7:c.*84G>A ENSP00000361359.3:n.*84G>A
ENST00000466205.5:c.820G>A
ENST00000489304.5:n.994G>A
ENST00000620709.4:c.*465G>A ENSP00000484074.1:n.*465G>A
NM_001250.5:c.*84G>A NP_001241.1:n.*84G>A
NM_001302753.1:c.*244G>A NP_001289682.1:n.*244G>A
NM_152854.3:c.*244G>A NP_690593.1:n.*244G>A
NR_126502.1:n.1011G>A
XM_005260617.2:c.*84G>A XP_005260674.1:n.*84G>A
XM_005260619.2:c.*84G>A XP_005260676.1:n.*84G>A
NM_001322421.1:c.*84G>A NP_001309350.1:n.*84G>A
NM_001322422.1:c.*84G>A NP_001309351.1:n.*84G>A
NM_001362758.1:c.*244G>A NP_001349687.1:n.*244G>A
NR_136327.1:n.914G>A
XM_005260619.3:c.*84G>A XP_005260676.1:n.*84G>A
XM_017028135.1:c.953G>A XP_016883624.1:p.Arg318Lys
XM_017028136.1:c.851G>A XP_016883625.1:p.Arg284Lys
NM_001250.6:c.*84G>A MANE Select NP_001241.1:n.*84G>A
NM_001302753.2:c.*244G>A NP_001289682.1:n.*244G>A
NM_001322421.2:c.*84G>A NP_001309350.1:n.*84G>A
NM_001322422.2:c.*84G>A NP_001309351.1:n.*84G>A
NM_001362758.2:c.*244G>A NP_001349687.1:n.*244G>A
NM_152854.4:c.*244G>A NP_690593.1:n.*244G>A
NR_126502.2:n.951G>A
NR_136327.2:n.854G>A