Canonical Allele Identifier: CA2366533269

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129169T= , CM000682.2:g.46129169T=	GRCh38
NC_000020.10:g.44757808T= , CM000682.1:g.44757808T=	GRCh37
NC_000020.9:g.44191215T=	NCBI36
NG_007279.1:g.15903T= , LRG_40:g.15903T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1046T=	ENSP00000512096.1:n.1046T=
ENST00000695675.1:n.2839T=
ENST00000372285.8:c.*129T= MANE Select	ENSP00000361359.3:n.*129T=
ENST00000372276.7:c.*289T=	ENSP00000361350.3:n.*289T=
ENST00000372285.7:c.*129T=	ENSP00000361359.3:n.*129T=
ENST00000489304.5:n.1039T=
ENST00000620709.4:c.*510T=	ENSP00000484074.1:n.*510T=
NM_001250.5:c.*129T=	NP_001241.1:n.*129T=
NM_001302753.1:c.*289T=	NP_001289682.1:n.*289T=
NM_152854.3:c.*289T=	NP_690593.1:n.*289T=
NR_126502.1:n.1056T=
XM_005260617.2:c.*129T=	XP_005260674.1:n.*129T=
XM_005260619.2:c.*129T=	XP_005260676.1:n.*129T=
NM_001322421.1:c.*129T=	NP_001309350.1:n.*129T=
NM_001322422.1:c.*129T=	NP_001309351.1:n.*129T=
NM_001362758.1:c.*289T=	NP_001349687.1:n.*289T=
NR_136327.1:n.959T=
XM_005260619.3:c.*129T=	XP_005260676.1:n.*129T=
XM_017028135.1:c.*26T=	XP_016883624.1:n.*26T=
XM_017028136.1:c.*26T=	XP_016883625.1:n.*26T=
NM_001250.6:c.*129T= MANE Select	NP_001241.1:n.*129T=
NM_001302753.2:c.*289T=	NP_001289682.1:n.*289T=
NM_001322421.2:c.*129T=	NP_001309350.1:n.*129T=
NM_001322422.2:c.*129T=	NP_001309351.1:n.*129T=
NM_001362758.2:c.*289T=	NP_001349687.1:n.*289T=
NM_152854.4:c.*289T=	NP_690593.1:n.*289T=
NR_126502.2:n.996T=
NR_136327.2:n.899T=