Canonical Allele Identifier: CA2366533239

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129126G= , CM000682.2:g.46129126G=	GRCh38
NC_000020.10:g.44757765G= , CM000682.1:g.44757765G=	GRCh37
NC_000020.9:g.44191172G=	NCBI36
NG_007279.1:g.15860G= , LRG_40:g.15860G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1003G=	ENSP00000512096.1:n.1003G=
ENST00000695675.1:n.2796G=
ENST00000372285.8:c.*86G= MANE Select	ENSP00000361359.3:n.*86G=
ENST00000372276.7:c.*246G=	ENSP00000361350.3:n.*246G=
ENST00000372285.7:c.*86G=	ENSP00000361359.3:n.*86G=
ENST00000466205.5:c.822G=
ENST00000489304.5:n.996G=
ENST00000620709.4:c.*467G=	ENSP00000484074.1:n.*467G=
NM_001250.5:c.*86G=	NP_001241.1:n.*86G=
NM_001302753.1:c.*246G=	NP_001289682.1:n.*246G=
NM_152854.3:c.*246G=	NP_690593.1:n.*246G=
NR_126502.1:n.1013G=
XM_005260617.2:c.*86G=	XP_005260674.1:n.*86G=
XM_005260619.2:c.*86G=	XP_005260676.1:n.*86G=
NM_001322421.1:c.*86G=	NP_001309350.1:n.*86G=
NM_001322422.1:c.*86G=	NP_001309351.1:n.*86G=
NM_001362758.1:c.*246G=	NP_001349687.1:n.*246G=
NR_136327.1:n.916G=
XM_005260619.3:c.*86G=	XP_005260676.1:n.*86G=
XM_017028135.1:c.955G=	XP_016883624.1:p.Val319=
XM_017028136.1:c.853G=	XP_016883625.1:p.Val285=
NM_001250.6:c.*86G= MANE Select	NP_001241.1:n.*86G=
NM_001302753.2:c.*246G=	NP_001289682.1:n.*246G=
NM_001322421.2:c.*86G=	NP_001309350.1:n.*86G=
NM_001322422.2:c.*86G=	NP_001309351.1:n.*86G=
NM_001362758.2:c.*246G=	NP_001349687.1:n.*246G=
NM_152854.4:c.*246G=	NP_690593.1:n.*246G=
NR_126502.2:n.953G=
NR_136327.2:n.856G=