Canonical Allele Identifier: CA2366533216

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129095A= , CM000682.2:g.46129095A=	GRCh38
NC_000020.10:g.44757734A= , CM000682.1:g.44757734A=	GRCh37
NC_000020.9:g.44191141A=	NCBI36
NG_007279.1:g.15829A= , LRG_40:g.15829A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.972A=	ENSP00000512096.1:n.972A=
ENST00000695675.1:n.2765A=
ENST00000372285.8:c.*55A= MANE Select	ENSP00000361359.3:n.*55A=
ENST00000372276.7:c.*215A=	ENSP00000361350.3:n.*215A=
ENST00000372285.7:c.*55A=	ENSP00000361359.3:n.*55A=
ENST00000466205.5:c.791A=
ENST00000489304.5:n.965A=
ENST00000620709.4:c.*436A=	ENSP00000484074.1:n.*436A=
NM_001250.5:c.*55A=	NP_001241.1:n.*55A=
NM_001302753.1:c.*215A=	NP_001289682.1:n.*215A=
NM_152854.3:c.*215A=	NP_690593.1:n.*215A=
NR_126502.1:n.982A=
XM_005260617.2:c.*55A=	XP_005260674.1:n.*55A=
XM_005260619.2:c.*55A=	XP_005260676.1:n.*55A=
NM_001322421.1:c.*55A=	NP_001309350.1:n.*55A=
NM_001322422.1:c.*55A=	NP_001309351.1:n.*55A=
NM_001362758.1:c.*215A=	NP_001349687.1:n.*215A=
NR_136327.1:n.885A=
XM_005260619.3:c.*55A=	XP_005260676.1:n.*55A=
XM_017028135.1:c.924A=	XP_016883624.1:p.Arg308=
XM_017028136.1:c.822A=	XP_016883625.1:p.Arg274=
NM_001250.6:c.*55A= MANE Select	NP_001241.1:n.*55A=
NM_001302753.2:c.*215A=	NP_001289682.1:n.*215A=
NM_001322421.2:c.*55A=	NP_001309350.1:n.*55A=
NM_001322422.2:c.*55A=	NP_001309351.1:n.*55A=
NM_001362758.2:c.*215A=	NP_001349687.1:n.*215A=
NM_152854.4:c.*215A=	NP_690593.1:n.*215A=
NR_126502.2:n.922A=
NR_136327.2:n.825A=