Canonical Allele Identifier: CA409205646
Gene: CD40 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46122736G>A , CM000682.2:g.46122736G>A GRCh38
NC_000020.10:g.44751375G>A , CM000682.1:g.44751375G>A GRCh37
NC_000020.9:g.44184782G>A NCBI36
NG_007279.1:g.9470G>A , LRG_40:g.9470G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.479G>A ENSP00000512095.1:n.479G>A
ENST00000489304.6:c.383G>A ENSP00000512096.1:p.Gly128Asp
ENST00000695669.1:n.456G>A
ENST00000695670.1:n.363G>A
ENST00000695671.1:c.383G>A ENSP00000512093.1:p.Gly128Asp
ENST00000695672.1:n.308G>A
ENST00000695673.1:n.248G>A
ENST00000372285.8:c.383G>A MANE Select ENSP00000361359.3:p.Gly128Asp
ENST00000372276.7:c.383G>A ENSP00000361350.3:p.Gly128Asp
ENST00000372285.7:c.383G>A ENSP00000361359.3:p.Gly128Asp
ENST00000461171.1:n.168G>A
ENST00000466205.5:c.379G>A
ENST00000477696.5:n.450G>A
ENST00000489304.5:n.376G>A
ENST00000620709.4:c.383G>A ENSP00000484074.1:p.Gly128Asp
NM_001250.5:c.383G>A NP_001241.1:p.Gly128Asp
NM_001302753.1:c.383G>A NP_001289682.1:p.Gly128Asp
NM_152854.3:c.383G>A NP_690593.1:p.Gly128Asp
NR_126502.1:n.473G>A
XM_005260617.2:c.383G>A XP_005260674.1:p.Gly128Asp
XM_005260619.2:c.383G>A XP_005260676.1:p.Gly128Asp
XM_011529109.1:c.383G>A XP_011527411.1:p.Gly128Asp
XR_936660.1:n.477G>A
NM_001322421.1:c.383G>A NP_001309350.1:p.Gly128Asp
NM_001322422.1:c.383G>A NP_001309351.1:p.Gly128Asp
NM_001362758.1:c.383G>A NP_001349687.1:p.Gly128Asp
NR_136327.1:n.473G>A
XM_005260619.3:c.383G>A XP_005260676.1:p.Gly128Asp
XM_011529109.2:c.383G>A XP_011527411.1:p.Gly128Asp
XM_017028135.1:c.383G>A XP_016883624.1:p.Gly128Asp
XM_017028136.1:c.383G>A XP_016883625.1:p.Gly128Asp
NM_001250.6:c.383G>A MANE Select NP_001241.1:p.Gly128Asp
NM_001302753.2:c.383G>A NP_001289682.1:p.Gly128Asp
NM_001322421.2:c.383G>A NP_001309350.1:p.Gly128Asp
NM_001322422.2:c.383G>A NP_001309351.1:p.Gly128Asp
NM_001362758.2:c.383G>A NP_001349687.1:p.Gly128Asp
NM_152854.4:c.383G>A NP_690593.1:p.Gly128Asp
NR_126502.2:n.413G>A
NR_136327.2:n.413G>A