Canonical Allele Identifier: CA409205074
Gene: CD40 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46122678T>A , CM000682.2:g.46122678T>A GRCh38
NC_000020.10:g.44751317T>A , CM000682.1:g.44751317T>A GRCh37
NC_000020.9:g.44184724T>A NCBI36
NG_007279.1:g.9412T>A , LRG_40:g.9412T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.421T>A ENSP00000512095.1:n.421T>A
ENST00000489304.6:c.325T>A ENSP00000512096.1:p.Trp109Arg
ENST00000695669.1:n.398T>A
ENST00000695670.1:n.305T>A
ENST00000695671.1:c.325T>A ENSP00000512093.1:p.Trp109Arg
ENST00000695672.1:n.250T>A
ENST00000695673.1:n.190T>A
ENST00000372285.8:c.325T>A MANE Select ENSP00000361359.3:p.Trp109Arg
ENST00000372276.7:c.325T>A ENSP00000361350.3:p.Trp109Arg
ENST00000372285.7:c.325T>A ENSP00000361359.3:p.Trp109Arg
ENST00000461171.1:n.110T>A
ENST00000466205.5:c.321T>A
ENST00000477696.5:n.392T>A
ENST00000489304.5:n.318T>A
ENST00000620709.4:c.325T>A ENSP00000484074.1:p.Trp109Arg
NM_001250.5:c.325T>A NP_001241.1:p.Trp109Arg
NM_001302753.1:c.325T>A NP_001289682.1:p.Trp109Arg
NM_152854.3:c.325T>A NP_690593.1:p.Trp109Arg
NR_126502.1:n.415T>A
XM_005260617.2:c.325T>A XP_005260674.1:p.Trp109Arg
XM_005260619.2:c.325T>A XP_005260676.1:p.Trp109Arg
XM_011529109.1:c.325T>A XP_011527411.1:p.Trp109Arg
XR_936660.1:n.419T>A
NM_001322421.1:c.325T>A NP_001309350.1:p.Trp109Arg
NM_001322422.1:c.325T>A NP_001309351.1:p.Trp109Arg
NM_001362758.1:c.325T>A NP_001349687.1:p.Trp109Arg
NR_136327.1:n.415T>A
XM_005260619.3:c.325T>A XP_005260676.1:p.Trp109Arg
XM_011529109.2:c.325T>A XP_011527411.1:p.Trp109Arg
XM_017028135.1:c.325T>A XP_016883624.1:p.Trp109Arg
XM_017028136.1:c.325T>A XP_016883625.1:p.Trp109Arg
NM_001250.6:c.325T>A MANE Select NP_001241.1:p.Trp109Arg
NM_001302753.2:c.325T>A NP_001289682.1:p.Trp109Arg
NM_001322421.2:c.325T>A NP_001309350.1:p.Trp109Arg
NM_001322422.2:c.325T>A NP_001309351.1:p.Trp109Arg
NM_001362758.2:c.325T>A NP_001349687.1:p.Trp109Arg
NM_152854.4:c.325T>A NP_690593.1:p.Trp109Arg
NR_126502.2:n.355T>A
NR_136327.2:n.355T>A