Canonical Allele Identifier: CA2366533187

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129008G= , CM000682.2:g.46129008G=	GRCh38
NC_000020.10:g.44757647G= , CM000682.1:g.44757647G=	GRCh37
NC_000020.9:g.44191054G=	NCBI36
NG_007279.1:g.15742G= , LRG_40:g.15742G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.885G=	ENSP00000512096.1:n.885G=
ENST00000695675.1:n.2678G=
ENST00000372285.8:c.802G= MANE Select	ENSP00000361359.3:p.Glu268=
ENST00000372276.7:c.*128G=	ENSP00000361350.3:n.*128G=
ENST00000372285.7:c.802G=	ENSP00000361359.3:p.Glu268=
ENST00000466205.5:c.704G=
ENST00000489304.5:n.878G=
ENST00000620709.4:c.*349G=	ENSP00000484074.1:n.*349G=
NM_001250.5:c.802G=	NP_001241.1:p.Glu268=
NM_001302753.1:c.*128G=	NP_001289682.1:n.*128G=
NM_152854.3:c.*128G=	NP_690593.1:n.*128G=
NR_126502.1:n.895G=
XM_005260617.2:c.814G=	XP_005260674.1:p.Glu272=
XM_005260619.2:c.658G=	XP_005260676.1:p.Glu220=
XR_936660.1:n.802G=
NM_001322421.1:c.814G=	NP_001309350.1:p.Glu272=
NM_001322422.1:c.646G=	NP_001309351.1:p.Glu216=
NM_001362758.1:c.*128G=	NP_001349687.1:n.*128G=
NR_136327.1:n.798G=
XM_005260619.3:c.658G=	XP_005260676.1:p.Glu220=
XM_017028135.1:c.837G=	XP_016883624.1:p.Lys279=
XM_017028136.1:c.735G=	XP_016883625.1:p.Lys245=
NM_001250.6:c.802G= MANE Select	NP_001241.1:p.Glu268=
NM_001302753.2:c.*128G=	NP_001289682.1:n.*128G=
NM_001322421.2:c.814G=	NP_001309350.1:p.Glu272=
NM_001322422.2:c.646G=	NP_001309351.1:p.Glu216=
NM_001362758.2:c.*128G=	NP_001349687.1:n.*128G=
NM_152854.4:c.*128G=	NP_690593.1:n.*128G=
NR_126502.2:n.835G=
NR_136327.2:n.738G=