Canonical Allele Identifier: CA2366533193

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129025G= , CM000682.2:g.46129025G=	GRCh38
NC_000020.10:g.44757664G= , CM000682.1:g.44757664G=	GRCh37
NC_000020.9:g.44191071G=	NCBI36
NG_007279.1:g.15759G= , LRG_40:g.15759G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.902G=	ENSP00000512096.1:n.902G=
ENST00000695675.1:n.2695G=
ENST00000372285.8:c.819G= MANE Select	ENSP00000361359.3:p.Val273=
ENST00000372276.7:c.*145G=	ENSP00000361350.3:n.*145G=
ENST00000372285.7:c.819G=	ENSP00000361359.3:p.Val273=
ENST00000466205.5:c.721G=
ENST00000489304.5:n.895G=
ENST00000620709.4:c.*366G=	ENSP00000484074.1:n.*366G=
NM_001250.5:c.819G=	NP_001241.1:p.Val273=
NM_001302753.1:c.*145G=	NP_001289682.1:n.*145G=
NM_152854.3:c.*145G=	NP_690593.1:n.*145G=
NR_126502.1:n.912G=
XM_005260617.2:c.831G=	XP_005260674.1:p.Val277=
XM_005260619.2:c.675G=	XP_005260676.1:p.Val225=
XR_936660.1:n.819G=
NM_001322421.1:c.831G=	NP_001309350.1:p.Val277=
NM_001322422.1:c.663G=	NP_001309351.1:p.Val221=
NM_001362758.1:c.*145G=	NP_001349687.1:n.*145G=
NR_136327.1:n.815G=
XM_005260619.3:c.675G=	XP_005260676.1:p.Val225=
XM_017028135.1:c.854G=	XP_016883624.1:p.Cys285=
XM_017028136.1:c.752G=	XP_016883625.1:p.Cys251=
NM_001250.6:c.819G= MANE Select	NP_001241.1:p.Val273=
NM_001302753.2:c.*145G=	NP_001289682.1:n.*145G=
NM_001322421.2:c.831G=	NP_001309350.1:p.Val277=
NM_001322422.2:c.663G=	NP_001309351.1:p.Val221=
NM_001362758.2:c.*145G=	NP_001349687.1:n.*145G=
NM_152854.4:c.*145G=	NP_690593.1:n.*145G=
NR_126502.2:n.852G=
NR_136327.2:n.755G=