Canonical Allele Identifier: CA409212206
Gene: CD40 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46128999G>A , CM000682.2:g.46128999G>A GRCh38
NC_000020.10:g.44757638G>A , CM000682.1:g.44757638G>A GRCh37
NC_000020.9:g.44191045G>A NCBI36
NG_007279.1:g.15733G>A , LRG_40:g.15733G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.795G>A ENSP00000512095.1:n.795G>A
ENST00000489304.6:c.876G>A ENSP00000512096.1:n.876G>A
ENST00000695675.1:n.2669G>A
ENST00000372285.8:c.793G>A MANE Select ENSP00000361359.3:p.Asp265Asn
ENST00000372276.7:c.*119G>A ENSP00000361350.3:n.*119G>A
ENST00000372285.7:c.793G>A ENSP00000361359.3:p.Asp265Asn
ENST00000466205.5:c.695G>A
ENST00000477696.5:n.766G>A
ENST00000489304.5:n.869G>A
ENST00000620709.4:c.*340G>A ENSP00000484074.1:n.*340G>A
NM_001250.5:c.793G>A NP_001241.1:p.Asp265Asn
NM_001302753.1:c.*119G>A NP_001289682.1:n.*119G>A
NM_152854.3:c.*119G>A NP_690593.1:n.*119G>A
NR_126502.1:n.886G>A
XM_005260617.2:c.805G>A XP_005260674.1:p.Asp269Asn
XM_005260619.2:c.649G>A XP_005260676.1:p.Asp217Asn
XR_936660.1:n.793G>A
NM_001322421.1:c.805G>A NP_001309350.1:p.Asp269Asn
NM_001322422.1:c.637G>A NP_001309351.1:p.Asp213Asn
NM_001362758.1:c.*119G>A NP_001349687.1:n.*119G>A
NR_136327.1:n.789G>A
XM_005260619.3:c.649G>A XP_005260676.1:p.Asp217Asn
XM_017028135.1:c.828G>A XP_016883624.1:p.Arg276=
XM_017028136.1:c.726G>A XP_016883625.1:p.Arg242=
NM_001250.6:c.793G>A MANE Select NP_001241.1:p.Asp265Asn
NM_001302753.2:c.*119G>A NP_001289682.1:n.*119G>A
NM_001322421.2:c.805G>A NP_001309350.1:p.Asp269Asn
NM_001322422.2:c.637G>A NP_001309351.1:p.Asp213Asn
NM_001362758.2:c.*119G>A NP_001349687.1:n.*119G>A
NM_152854.4:c.*119G>A NP_690593.1:n.*119G>A
NR_126502.2:n.826G>A
NR_136327.2:n.729G>A