Canonical Allele Identifier: CA2653134160

Gene: CD40

Linked Data

• gnomAD v4: 20-46129189-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129189C>G , CM000682.2:g.46129189C>G	GRCh38
NC_000020.10:g.44757828C>G , CM000682.1:g.44757828C>G	GRCh37
NC_000020.9:g.44191235C>G	NCBI36
NG_007279.1:g.15923C>G , LRG_40:g.15923C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1066C>G	ENSP00000512096.1:n.1066C>G
ENST00000695675.1:n.2859C>G
ENST00000372285.8:c.*149C>G MANE Select	ENSP00000361359.3:n.*149C>G
ENST00000372276.7:c.*309C>G	ENSP00000361350.3:n.*309C>G
ENST00000372285.7:c.*149C>G	ENSP00000361359.3:n.*149C>G
ENST00000489304.5:n.1059C>G
ENST00000620709.4:c.*530C>G	ENSP00000484074.1:n.*530C>G
NM_001250.5:c.*149C>G	NP_001241.1:n.*149C>G
NM_001302753.1:c.*309C>G	NP_001289682.1:n.*309C>G
NM_152854.3:c.*309C>G	NP_690593.1:n.*309C>G
NR_126502.1:n.1076C>G
XM_005260617.2:c.*149C>G	XP_005260674.1:n.*149C>G
XM_005260619.2:c.*149C>G	XP_005260676.1:n.*149C>G
NM_001322421.1:c.*149C>G	NP_001309350.1:n.*149C>G
NM_001322422.1:c.*149C>G	NP_001309351.1:n.*149C>G
NM_001362758.1:c.*309C>G	NP_001349687.1:n.*309C>G
NR_136327.1:n.979C>G
XM_005260619.3:c.*149C>G	XP_005260676.1:n.*149C>G
XM_017028135.1:c.*46C>G	XP_016883624.1:n.*46C>G
XM_017028136.1:c.*46C>G	XP_016883625.1:n.*46C>G
NM_001250.6:c.*149C>G MANE Select	NP_001241.1:n.*149C>G
NM_001302753.2:c.*309C>G	NP_001289682.1:n.*309C>G
NM_001322421.2:c.*149C>G	NP_001309350.1:n.*149C>G
NM_001322422.2:c.*149C>G	NP_001309351.1:n.*149C>G
NM_001362758.2:c.*309C>G	NP_001349687.1:n.*309C>G
NM_152854.4:c.*309C>G	NP_690593.1:n.*309C>G
NR_126502.2:n.1016C>G
NR_136327.2:n.919C>G