Canonical Allele Identifier: CA2839538560
Gene: CD40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118313dup , CM000682.2:g.46118313dup GRCh38
NC_000020.10:g.44746952dup , CM000682.1:g.44746952dup GRCh37
NC_000020.9:g.44180359dup NCBI36
NG_007279.1:g.5047dup , LRG_40:g.5047dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000695669.1:n.43dup
ENST00000695670.1:n.29dup
ENST00000372285.7:c.-31dup ENSP00000361359.3:n.-31dup
ENST00000620709.4:c.-31dup ENSP00000484074.1:n.-31dup
NM_001250.5:c.-31dup NP_001241.1:n.-31dup
NM_001302753.1:c.-31dup NP_001289682.1:n.-31dup
NM_152854.3:c.-31dup NP_690593.1:n.-31dup
NR_126502.1:n.60dup
XM_005260617.2:c.-31dup XP_005260674.1:n.-31dup
XM_005260619.2:c.-31dup XP_005260676.1:n.-31dup
XM_011529109.1:c.-31dup XP_011527411.1:n.-31dup
XR_936660.1:n.64dup
NM_001322421.1:c.-31dup NP_001309350.1:n.-31dup
NM_001322422.1:c.-31dup NP_001309351.1:n.-31dup
NM_001362758.1:c.-31dup NP_001349687.1:n.-31dup
NR_136327.1:n.60dup
XM_005260619.3:c.-31dup XP_005260676.1:n.-31dup
XM_011529109.2:c.-31dup XP_011527411.1:n.-31dup
XM_017028135.1:c.-31dup XP_016883624.1:n.-31dup
XM_017028136.1:c.-31dup XP_016883625.1:n.-31dup