Canonical Allele Identifier: CA2366530762

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46122711G= , CM000682.2:g.46122711G=	GRCh38
NC_000020.10:g.44751350G= , CM000682.1:g.44751350G=	GRCh37
NC_000020.9:g.44184757G=	NCBI36
NG_007279.1:g.9445G= , LRG_40:g.9445G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.454G=	ENSP00000512095.1:n.454G=
ENST00000489304.6:c.358G=	ENSP00000512096.1:p.Val120=
ENST00000695669.1:n.431G=
ENST00000695670.1:n.338G=
ENST00000695671.1:c.358G=	ENSP00000512093.1:p.Val120=
ENST00000695672.1:n.283G=
ENST00000695673.1:n.223G=
ENST00000372285.8:c.358G= MANE Select	ENSP00000361359.3:p.Val120=
ENST00000372276.7:c.358G=	ENSP00000361350.3:p.Val120=
ENST00000372285.7:c.358G=	ENSP00000361359.3:p.Val120=
ENST00000461171.1:n.143G=
ENST00000466205.5:c.354G=
ENST00000477696.5:n.425G=
ENST00000489304.5:n.351G=
ENST00000620709.4:c.358G=	ENSP00000484074.1:p.Val120=
NM_001250.5:c.358G=	NP_001241.1:p.Val120=
NM_001302753.1:c.358G=	NP_001289682.1:p.Val120=
NM_152854.3:c.358G=	NP_690593.1:p.Val120=
NR_126502.1:n.448G=
XM_005260617.2:c.358G=	XP_005260674.1:p.Val120=
XM_005260619.2:c.358G=	XP_005260676.1:p.Val120=
XM_011529109.1:c.358G=	XP_011527411.1:p.Val120=
XR_936660.1:n.452G=
NM_001322421.1:c.358G=	NP_001309350.1:p.Val120=
NM_001322422.1:c.358G=	NP_001309351.1:p.Val120=
NM_001362758.1:c.358G=	NP_001349687.1:p.Val120=
NR_136327.1:n.448G=
XM_005260619.3:c.358G=	XP_005260676.1:p.Val120=
XM_011529109.2:c.358G=	XP_011527411.1:p.Val120=
XM_017028135.1:c.358G=	XP_016883624.1:p.Val120=
XM_017028136.1:c.358G=	XP_016883625.1:p.Val120=
NM_001250.6:c.358G= MANE Select	NP_001241.1:p.Val120=
NM_001302753.2:c.358G=	NP_001289682.1:p.Val120=
NM_001322421.2:c.358G=	NP_001309350.1:p.Val120=
NM_001322422.2:c.358G=	NP_001309351.1:p.Val120=
NM_001362758.2:c.358G=	NP_001349687.1:p.Val120=
NM_152854.4:c.358G=	NP_690593.1:p.Val120=
NR_126502.2:n.388G=
NR_136327.2:n.388G=