Canonical Allele Identifier: CA2366533248

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129133G= , CM000682.2:g.46129133G=	GRCh38
NC_000020.10:g.44757772G= , CM000682.1:g.44757772G=	GRCh37
NC_000020.9:g.44191179G=	NCBI36
NG_007279.1:g.15867G= , LRG_40:g.15867G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1010G=	ENSP00000512096.1:n.1010G=
ENST00000695675.1:n.2803G=
ENST00000372285.8:c.*93G= MANE Select	ENSP00000361359.3:n.*93G=
ENST00000372276.7:c.*253G=	ENSP00000361350.3:n.*253G=
ENST00000372285.7:c.*93G=	ENSP00000361359.3:n.*93G=
ENST00000489304.5:n.1003G=
ENST00000620709.4:c.*474G=	ENSP00000484074.1:n.*474G=
NM_001250.5:c.*93G=	NP_001241.1:n.*93G=
NM_001302753.1:c.*253G=	NP_001289682.1:n.*253G=
NM_152854.3:c.*253G=	NP_690593.1:n.*253G=
NR_126502.1:n.1020G=
XM_005260617.2:c.*93G=	XP_005260674.1:n.*93G=
XM_005260619.2:c.*93G=	XP_005260676.1:n.*93G=
NM_001322421.1:c.*93G=	NP_001309350.1:n.*93G=
NM_001322422.1:c.*93G=	NP_001309351.1:n.*93G=
NM_001362758.1:c.*253G=	NP_001349687.1:n.*253G=
NR_136327.1:n.923G=
XM_005260619.3:c.*93G=	XP_005260676.1:n.*93G=
XM_017028135.1:c.962G=	XP_016883624.1:p.Gly321=
XM_017028136.1:c.860G=	XP_016883625.1:p.Gly287=
NM_001250.6:c.*93G= MANE Select	NP_001241.1:n.*93G=
NM_001302753.2:c.*253G=	NP_001289682.1:n.*253G=
NM_001322421.2:c.*93G=	NP_001309350.1:n.*93G=
NM_001322422.2:c.*93G=	NP_001309351.1:n.*93G=
NM_001362758.2:c.*253G=	NP_001349687.1:n.*253G=
NM_152854.4:c.*253G=	NP_690593.1:n.*253G=
NR_126502.2:n.960G=
NR_136327.2:n.863G=