Canonical Allele Identifier: CA2366533303

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129207A= , CM000682.2:g.46129207A=	GRCh38
NC_000020.10:g.44757846A= , CM000682.1:g.44757846A=	GRCh37
NC_000020.9:g.44191253A=	NCBI36
NG_007279.1:g.15941A= , LRG_40:g.15941A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1084A=	ENSP00000512096.1:n.1084A=
ENST00000695675.1:n.2877A=
ENST00000372285.8:c.*167A= MANE Select	ENSP00000361359.3:n.*167A=
ENST00000372276.7:c.*327A=	ENSP00000361350.3:n.*327A=
ENST00000372285.7:c.*167A=	ENSP00000361359.3:n.*167A=
ENST00000489304.5:n.1077A=
ENST00000620709.4:c.*548A=	ENSP00000484074.1:n.*548A=
NM_001250.5:c.*167A=	NP_001241.1:n.*167A=
NM_001302753.1:c.*327A=	NP_001289682.1:n.*327A=
NM_152854.3:c.*327A=	NP_690593.1:n.*327A=
NR_126502.1:n.1094A=
XM_005260617.2:c.*167A=	XP_005260674.1:n.*167A=
XM_005260619.2:c.*167A=	XP_005260676.1:n.*167A=
NM_001322421.1:c.*167A=	NP_001309350.1:n.*167A=
NM_001322422.1:c.*167A=	NP_001309351.1:n.*167A=
NM_001362758.1:c.*327A=	NP_001349687.1:n.*327A=
NR_136327.1:n.997A=
XM_005260619.3:c.*167A=	XP_005260676.1:n.*167A=
XM_017028135.1:c.*64A=	XP_016883624.1:n.*64A=
XM_017028136.1:c.*64A=	XP_016883625.1:n.*64A=
NM_001250.6:c.*167A= MANE Select	NP_001241.1:n.*167A=
NM_001302753.2:c.*327A=	NP_001289682.1:n.*327A=
NM_001322421.2:c.*167A=	NP_001309350.1:n.*167A=
NM_001322422.2:c.*167A=	NP_001309351.1:n.*167A=
NM_001362758.2:c.*327A=	NP_001349687.1:n.*327A=
NM_152854.4:c.*327A=	NP_690593.1:n.*327A=
NR_126502.2:n.1034A=
NR_136327.2:n.937A=