Canonical Allele Identifier: CA2366528972
Gene: CD40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118271A= , CM000682.2:g.46118271A= GRCh38
NC_000020.10:g.44746910A= , CM000682.1:g.44746910A= GRCh37
NC_000020.9:g.44180317A= NCBI36
NG_007279.1:g.5005A= , LRG_40:g.5005A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695669.1:n.1A=
NM_001250.5:c.-73A= NP_001241.1:n.-73A=
NM_001302753.1:c.-73A= NP_001289682.1:n.-73A=
NM_152854.3:c.-73A= NP_690593.1:n.-73A=
NR_126502.1:n.18A=
XM_005260617.2:c.-73A= XP_005260674.1:n.-73A=
XM_005260619.2:c.-73A= XP_005260676.1:n.-73A=
XM_011529109.1:c.-73A= XP_011527411.1:n.-73A=
XR_936660.1:n.22A=
NM_001322421.1:c.-73A= NP_001309350.1:n.-73A=
NM_001322422.1:c.-73A= NP_001309351.1:n.-73A=
NM_001362758.1:c.-73A= NP_001349687.1:n.-73A=
NR_136327.1:n.18A=
XM_005260619.3:c.-73A= XP_005260676.1:n.-73A=
XM_011529109.2:c.-73A= XP_011527411.1:n.-73A=
XM_017028135.1:c.-73A= XP_016883624.1:n.-73A=
XM_017028136.1:c.-73A= XP_016883625.1:n.-73A=