Canonical Allele Identifier: CA2739725298

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129049C>A , CM000682.2:g.46129049C>A	GRCh38
NC_000020.10:g.44757688C>A , CM000682.1:g.44757688C>A	GRCh37
NC_000020.9:g.44191095C>A	NCBI36
NG_007279.1:g.15783C>A , LRG_40:g.15783C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.926C>A	ENSP00000512096.1:n.926C>A
ENST00000695675.1:n.2719C>A
ENST00000372285.8:c.*9C>A MANE Select	ENSP00000361359.3:n.*9C>A
ENST00000372276.7:c.*169C>A	ENSP00000361350.3:n.*169C>A
ENST00000372285.7:c.*9C>A	ENSP00000361359.3:n.*9C>A
ENST00000466205.5:c.745C>A
ENST00000489304.5:n.919C>A
ENST00000620709.4:c.*390C>A	ENSP00000484074.1:n.*390C>A
NM_001250.5:c.*9C>A	NP_001241.1:n.*9C>A
NM_001302753.1:c.*169C>A	NP_001289682.1:n.*169C>A
NM_152854.3:c.*169C>A	NP_690593.1:n.*169C>A
NR_126502.1:n.936C>A
XM_005260617.2:c.*9C>A	XP_005260674.1:n.*9C>A
XM_005260619.2:c.*9C>A	XP_005260676.1:n.*9C>A
XR_936660.1:n.843C>A
NM_001322421.1:c.*9C>A	NP_001309350.1:n.*9C>A
NM_001322422.1:c.*9C>A	NP_001309351.1:n.*9C>A
NM_001362758.1:c.*169C>A	NP_001349687.1:n.*169C>A
NR_136327.1:n.839C>A
XM_005260619.3:c.*9C>A	XP_005260676.1:n.*9C>A
XM_017028135.1:c.878C>A	XP_016883624.1:p.Pro293His
XM_017028136.1:c.776C>A	XP_016883625.1:p.Pro259His
NM_001250.6:c.*9C>A MANE Select	NP_001241.1:n.*9C>A
NM_001302753.2:c.*169C>A	NP_001289682.1:n.*169C>A
NM_001322421.2:c.*9C>A	NP_001309350.1:n.*9C>A
NM_001322422.2:c.*9C>A	NP_001309351.1:n.*9C>A
NM_001362758.2:c.*169C>A	NP_001349687.1:n.*169C>A
NM_152854.4:c.*169C>A	NP_690593.1:n.*169C>A
NR_126502.2:n.876C>A
NR_136327.2:n.779C>A