Canonical Allele Identifier: CA2366533197

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129044T= , CM000682.2:g.46129044T=	GRCh38
NC_000020.10:g.44757683T= , CM000682.1:g.44757683T=	GRCh37
NC_000020.9:g.44191090T=	NCBI36
NG_007279.1:g.15778T= , LRG_40:g.15778T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.921T=	ENSP00000512096.1:n.921T=
ENST00000695675.1:n.2714T=
ENST00000372285.8:c.*4T= MANE Select	ENSP00000361359.3:n.*4T=
ENST00000372276.7:c.*164T=	ENSP00000361350.3:n.*164T=
ENST00000372285.7:c.*4T=	ENSP00000361359.3:n.*4T=
ENST00000466205.5:c.740T=
ENST00000489304.5:n.914T=
ENST00000620709.4:c.*385T=	ENSP00000484074.1:n.*385T=
NM_001250.5:c.*4T=	NP_001241.1:n.*4T=
NM_001302753.1:c.*164T=	NP_001289682.1:n.*164T=
NM_152854.3:c.*164T=	NP_690593.1:n.*164T=
NR_126502.1:n.931T=
XM_005260617.2:c.*4T=	XP_005260674.1:n.*4T=
XM_005260619.2:c.*4T=	XP_005260676.1:n.*4T=
XR_936660.1:n.838T=
NM_001322421.1:c.*4T=	NP_001309350.1:n.*4T=
NM_001322422.1:c.*4T=	NP_001309351.1:n.*4T=
NM_001362758.1:c.*164T=	NP_001349687.1:n.*164T=
NR_136327.1:n.834T=
XM_005260619.3:c.*4T=	XP_005260676.1:n.*4T=
XM_017028135.1:c.873T=	XP_016883624.1:p.Ala291=
XM_017028136.1:c.771T=	XP_016883625.1:p.Ala257=
NM_001250.6:c.*4T= MANE Select	NP_001241.1:n.*4T=
NM_001302753.2:c.*164T=	NP_001289682.1:n.*164T=
NM_001322421.2:c.*4T=	NP_001309350.1:n.*4T=
NM_001322422.2:c.*4T=	NP_001309351.1:n.*4T=
NM_001362758.2:c.*164T=	NP_001349687.1:n.*164T=
NM_152854.4:c.*164T=	NP_690593.1:n.*164T=
NR_126502.2:n.871T=
NR_136327.2:n.774T=