Canonical Allele Identifier: CA2653131536

Gene: CD40

Linked Data

• gnomAD v4: 20-46118273-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46118273G>A , CM000682.2:g.46118273G>A	GRCh38
NC_000020.10:g.44746912G>A , CM000682.1:g.44746912G>A	GRCh37
NC_000020.9:g.44180319G>A	NCBI36
NG_007279.1:g.5007G>A , LRG_40:g.5007G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695669.1:n.3G>A
ENST00000372285.7:c.-71G>A	ENSP00000361359.3:n.-71G>A
NM_001250.5:c.-71G>A	NP_001241.1:n.-71G>A
NM_001302753.1:c.-71G>A	NP_001289682.1:n.-71G>A
NM_152854.3:c.-71G>A	NP_690593.1:n.-71G>A
NR_126502.1:n.20G>A
XM_005260617.2:c.-71G>A	XP_005260674.1:n.-71G>A
XM_005260619.2:c.-71G>A	XP_005260676.1:n.-71G>A
XM_011529109.1:c.-71G>A	XP_011527411.1:n.-71G>A
XR_936660.1:n.24G>A
NM_001322421.1:c.-71G>A	NP_001309350.1:n.-71G>A
NM_001322422.1:c.-71G>A	NP_001309351.1:n.-71G>A
NM_001362758.1:c.-71G>A	NP_001349687.1:n.-71G>A
NR_136327.1:n.20G>A
XM_005260619.3:c.-71G>A	XP_005260676.1:n.-71G>A
XM_011529109.2:c.-71G>A	XP_011527411.1:n.-71G>A
XM_017028135.1:c.-71G>A	XP_016883624.1:n.-71G>A
XM_017028136.1:c.-71G>A	XP_016883625.1:n.-71G>A