Canonical Allele Identifier: CA2366533099

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128225G= , CM000682.2:g.46128225G=	GRCh38
NC_000020.10:g.44756864G= , CM000682.1:g.44756864G=	GRCh37
NC_000020.9:g.44190271G=	NCBI36
NG_007279.1:g.14959G= , LRG_40:g.14959G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.648+1G=	ENSP00000512095.1:n.648+1G=
ENST00000489304.6:c.729+1G=	ENSP00000512096.1:n.729+1G=
ENST00000695670.1:n.616G=
ENST00000695671.1:c.686+1G=	ENSP00000512093.1:n.686+1G=
ENST00000695674.1:n.1125+1G=
ENST00000695675.1:n.2522+1G=
ENST00000372285.8:c.646+1G= MANE Select	ENSP00000361359.3:n.646+1G=
ENST00000372276.7:c.584+1G=	ENSP00000361350.3:n.584+1G=
ENST00000372285.7:c.646+1G=	ENSP00000361359.3:n.646+1G=
ENST00000466205.5:c.548+1G=
ENST00000477696.5:n.619+1G=
ENST00000489304.5:n.722+1G=
ENST00000620709.4:c.*193+1G=	ENSP00000484074.1:n.*193+1G=
NM_001250.5:c.646+1G=	NP_001241.1:n.646+1G=
NM_001302753.1:c.686+1G=	NP_001289682.1:n.686+1G=
NM_152854.3:c.584+1G=	NP_690593.1:n.584+1G=
NR_126502.1:n.739+1G=
XM_005260617.2:c.647G=	XP_005260674.1:p.Ser216=
XM_005260619.2:c.491G=	XP_005260676.1:p.Ser164=
XR_936660.1:n.646+1G=
NM_001322421.1:c.647G=	NP_001309350.1:p.Ser216=
NM_001322422.1:c.490+1G=	NP_001309351.1:n.490+1G=
NM_001362758.1:c.646+1G=	NP_001349687.1:n.646+1G=
NR_136327.1:n.642+1G=
XM_005260619.3:c.491G=	XP_005260676.1:p.Ser164=
XM_017028135.1:c.686+1G=	XP_016883624.1:n.686+1G=
XM_017028136.1:c.584+1G=	XP_016883625.1:n.584+1G=
NM_001250.6:c.646+1G= MANE Select	NP_001241.1:n.646+1G=
NM_001302753.2:c.686+1G=	NP_001289682.1:n.686+1G=
NM_001322421.2:c.647G=	NP_001309350.1:p.Ser216=
NM_001322422.2:c.490+1G=	NP_001309351.1:n.490+1G=
NM_001362758.2:c.646+1G=	NP_001349687.1:n.646+1G=
NM_152854.4:c.584+1G=	NP_690593.1:n.584+1G=
NR_126502.2:n.679+1G=
NR_136327.2:n.582+1G=