Canonical Allele Identifier: CA2366533719

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128893C= , CM000682.2:g.46128893C=	GRCh38
NC_000020.10:g.44757532C= , CM000682.1:g.44757532C=	GRCh37
NC_000020.9:g.44190939C=	NCBI36
NG_007279.1:g.15627C= , LRG_40:g.15627C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.689C=	ENSP00000512095.1:n.689C=
ENST00000489304.6:c.770C=	ENSP00000512096.1:n.770C=
ENST00000695675.1:n.2563C=
ENST00000372285.8:c.687C= MANE Select	ENSP00000361359.3:p.Pro229=
ENST00000372276.7:c.*13C=	ENSP00000361350.3:n.*13C=
ENST00000372285.7:c.687C=	ENSP00000361359.3:p.Pro229=
ENST00000466205.5:c.589C=
ENST00000477696.5:n.660C=
ENST00000489304.5:n.763C=
ENST00000620709.4:c.*234C=	ENSP00000484074.1:n.*234C=
NM_001250.5:c.687C=	NP_001241.1:p.Pro229=
NM_001302753.1:c.*13C=	NP_001289682.1:n.*13C=
NM_152854.3:c.*13C=	NP_690593.1:n.*13C=
NR_126502.1:n.780C=
XM_005260617.2:c.699C=	XP_005260674.1:p.Pro233=
XM_005260619.2:c.543C=	XP_005260676.1:p.Pro181=
XR_936660.1:n.687C=
NM_001322421.1:c.699C=	NP_001309350.1:p.Pro233=
NM_001322422.1:c.531C=	NP_001309351.1:p.Pro177=
NM_001362758.1:c.*13C=	NP_001349687.1:n.*13C=
NR_136327.1:n.683C=
XM_005260619.3:c.543C=	XP_005260676.1:p.Pro181=
XM_017028135.1:c.722C=	XP_016883624.1:p.Pro241=
XM_017028136.1:c.620C=	XP_016883625.1:p.Pro207=
NM_001250.6:c.687C= MANE Select	NP_001241.1:p.Pro229=
NM_001302753.2:c.*13C=	NP_001289682.1:n.*13C=
NM_001322421.2:c.699C=	NP_001309350.1:p.Pro233=
NM_001322422.2:c.531C=	NP_001309351.1:p.Pro177=
NM_001362758.2:c.*13C=	NP_001349687.1:n.*13C=
NM_152854.4:c.*13C=	NP_690593.1:n.*13C=
NR_126502.2:n.720C=
NR_136327.2:n.623C=