Canonical Allele Identifier: CA2366533288

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129188A= , CM000682.2:g.46129188A=	GRCh38
NC_000020.10:g.44757827A= , CM000682.1:g.44757827A=	GRCh37
NC_000020.9:g.44191234A=	NCBI36
NG_007279.1:g.15922A= , LRG_40:g.15922A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1065A=	ENSP00000512096.1:n.1065A=
ENST00000695675.1:n.2858A=
ENST00000372285.8:c.*148A= MANE Select	ENSP00000361359.3:n.*148A=
ENST00000372276.7:c.*308A=	ENSP00000361350.3:n.*308A=
ENST00000372285.7:c.*148A=	ENSP00000361359.3:n.*148A=
ENST00000489304.5:n.1058A=
ENST00000620709.4:c.*529A=	ENSP00000484074.1:n.*529A=
NM_001250.5:c.*148A=	NP_001241.1:n.*148A=
NM_001302753.1:c.*308A=	NP_001289682.1:n.*308A=
NM_152854.3:c.*308A=	NP_690593.1:n.*308A=
NR_126502.1:n.1075A=
XM_005260617.2:c.*148A=	XP_005260674.1:n.*148A=
XM_005260619.2:c.*148A=	XP_005260676.1:n.*148A=
NM_001322421.1:c.*148A=	NP_001309350.1:n.*148A=
NM_001322422.1:c.*148A=	NP_001309351.1:n.*148A=
NM_001362758.1:c.*308A=	NP_001349687.1:n.*308A=
NR_136327.1:n.978A=
XM_005260619.3:c.*148A=	XP_005260676.1:n.*148A=
XM_017028135.1:c.*45A=	XP_016883624.1:n.*45A=
XM_017028136.1:c.*45A=	XP_016883625.1:n.*45A=
NM_001250.6:c.*148A= MANE Select	NP_001241.1:n.*148A=
NM_001302753.2:c.*308A=	NP_001289682.1:n.*308A=
NM_001322421.2:c.*148A=	NP_001309350.1:n.*148A=
NM_001322422.2:c.*148A=	NP_001309351.1:n.*148A=
NM_001362758.2:c.*308A=	NP_001349687.1:n.*308A=
NM_152854.4:c.*308A=	NP_690593.1:n.*308A=
NR_126502.2:n.1015A=
NR_136327.2:n.918A=