Canonical Allele Identifier: CA2366533106
Gene: CD40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46128234C= , CM000682.2:g.46128234C= GRCh38
NC_000020.10:g.44756873C= , CM000682.1:g.44756873C= GRCh37
NC_000020.9:g.44190280C= NCBI36
NG_007279.1:g.14968C= , LRG_40:g.14968C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.648+10C= ENSP00000512095.1:n.648+10C=
ENST00000489304.6:c.729+10C= ENSP00000512096.1:n.729+10C=
ENST00000695670.1:n.625C=
ENST00000695671.1:c.686+10C= ENSP00000512093.1:n.686+10C=
ENST00000695674.1:n.1125+10C=
ENST00000695675.1:n.2522+10C=
ENST00000372285.8:c.646+10C= MANE Select ENSP00000361359.3:n.646+10C=
ENST00000372276.7:c.584+10C= ENSP00000361350.3:n.584+10C=
ENST00000372285.7:c.646+10C= ENSP00000361359.3:n.646+10C=
ENST00000466205.5:c.548+10C=
ENST00000477696.5:n.619+10C=
ENST00000489304.5:n.722+10C=
ENST00000620709.4:c.*193+10C= ENSP00000484074.1:n.*193+10C=
NM_001250.5:c.646+10C= NP_001241.1:n.646+10C=
NM_001302753.1:c.686+10C= NP_001289682.1:n.686+10C=
NM_152854.3:c.584+10C= NP_690593.1:n.584+10C=
NR_126502.1:n.739+10C=
XM_005260617.2:c.656C= XP_005260674.1:p.Ser219=
XM_005260619.2:c.500C= XP_005260676.1:p.Ser167=
XR_936660.1:n.646+10C=
NM_001322421.1:c.656C= NP_001309350.1:p.Ser219=
NM_001322422.1:c.490+10C= NP_001309351.1:n.490+10C=
NM_001362758.1:c.646+10C= NP_001349687.1:n.646+10C=
NR_136327.1:n.642+10C=
XM_005260619.3:c.500C= XP_005260676.1:p.Ser167=
XM_017028135.1:c.686+10C= XP_016883624.1:n.686+10C=
XM_017028136.1:c.584+10C= XP_016883625.1:n.584+10C=
NM_001250.6:c.646+10C= MANE Select NP_001241.1:n.646+10C=
NM_001302753.2:c.686+10C= NP_001289682.1:n.686+10C=
NM_001322421.2:c.656C= NP_001309350.1:p.Ser219=
NM_001322422.2:c.490+10C= NP_001309351.1:n.490+10C=
NM_001362758.2:c.646+10C= NP_001349687.1:n.646+10C=
NM_152854.4:c.584+10C= NP_690593.1:n.584+10C=
NR_126502.2:n.679+10C=
NR_136327.2:n.582+10C=