Canonical Allele Identifier: CA409211836
Gene: CD40 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46128937G>A , CM000682.2:g.46128937G>A GRCh38
NC_000020.10:g.44757576G>A , CM000682.1:g.44757576G>A GRCh37
NC_000020.9:g.44190983G>A NCBI36
NG_007279.1:g.15671G>A , LRG_40:g.15671G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.733G>A ENSP00000512095.1:n.733G>A
ENST00000489304.6:c.814G>A ENSP00000512096.1:n.814G>A
ENST00000695675.1:n.2607G>A
ENST00000372285.8:c.731G>A MANE Select ENSP00000361359.3:p.Gly244Asp
ENST00000372276.7:c.*57G>A ENSP00000361350.3:n.*57G>A
ENST00000372285.7:c.731G>A ENSP00000361359.3:p.Gly244Asp
ENST00000466205.5:c.633G>A
ENST00000477696.5:n.704G>A
ENST00000489304.5:n.807G>A
ENST00000620709.4:c.*278G>A ENSP00000484074.1:n.*278G>A
NM_001250.5:c.731G>A NP_001241.1:p.Gly244Asp
NM_001302753.1:c.*57G>A NP_001289682.1:n.*57G>A
NM_152854.3:c.*57G>A NP_690593.1:n.*57G>A
NR_126502.1:n.824G>A
XM_005260617.2:c.743G>A XP_005260674.1:p.Gly248Asp
XM_005260619.2:c.587G>A XP_005260676.1:p.Gly196Asp
XR_936660.1:n.731G>A
NM_001322421.1:c.743G>A NP_001309350.1:p.Gly248Asp
NM_001322422.1:c.575G>A NP_001309351.1:p.Gly192Asp
NM_001362758.1:c.*57G>A NP_001349687.1:n.*57G>A
NR_136327.1:n.727G>A
XM_005260619.3:c.587G>A XP_005260676.1:p.Gly196Asp
XM_017028135.1:c.766G>A XP_016883624.1:p.Ala256Thr
XM_017028136.1:c.664G>A XP_016883625.1:p.Ala222Thr
NM_001250.6:c.731G>A MANE Select NP_001241.1:p.Gly244Asp
NM_001302753.2:c.*57G>A NP_001289682.1:n.*57G>A
NM_001322421.2:c.743G>A NP_001309350.1:p.Gly248Asp
NM_001322422.2:c.575G>A NP_001309351.1:p.Gly192Asp
NM_001362758.2:c.*57G>A NP_001349687.1:n.*57G>A
NM_152854.4:c.*57G>A NP_690593.1:n.*57G>A
NR_126502.2:n.764G>A
NR_136327.2:n.667G>A