Canonical Allele Identifier: CA2366533139

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128280A= , CM000682.2:g.46128280A=	GRCh38
NC_000020.10:g.44756919A= , CM000682.1:g.44756919A=	GRCh37
NC_000020.9:g.44190326A=	NCBI36
NG_007279.1:g.15014A= , LRG_40:g.15014A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.649-50A=	ENSP00000512095.1:n.649-50A=
ENST00000489304.6:c.730-50A=	ENSP00000512096.1:n.730-50A=
ENST00000695670.1:n.627+44A=
ENST00000695671.1:c.687-50A=	ENSP00000512093.1:n.687-50A=
ENST00000695674.1:n.1126-50A=
ENST00000695675.1:n.2523-50A=
ENST00000372285.8:c.647-50A= MANE Select	ENSP00000361359.3:n.647-50A=
ENST00000372276.7:c.585-50A=	ENSP00000361350.3:n.585-50A=
ENST00000372285.7:c.647-50A=	ENSP00000361359.3:n.647-50A=
ENST00000466205.5:c.549-50A=
ENST00000477696.5:n.620-50A=
ENST00000489304.5:n.723-50A=
ENST00000620709.4:c.*194-50A=	ENSP00000484074.1:n.*194-50A=
NM_001250.5:c.647-50A=	NP_001241.1:n.647-50A=
NM_001302753.1:c.687-50A=	NP_001289682.1:n.687-50A=
NM_152854.3:c.585-50A=	NP_690593.1:n.585-50A=
NR_126502.1:n.740-50A=
XM_005260617.2:c.658+44A=	XP_005260674.1:n.658+44A=
XM_005260619.2:c.502+44A=	XP_005260676.1:n.502+44A=
XR_936660.1:n.647-50A=
NM_001322421.1:c.658+44A=	NP_001309350.1:n.658+44A=
NM_001322422.1:c.491-50A=	NP_001309351.1:n.491-50A=
NM_001362758.1:c.647-55A=	NP_001349687.1:n.647-55A=
NR_136327.1:n.643-50A=
XM_005260619.3:c.502+44A=	XP_005260676.1:n.502+44A=
XM_017028135.1:c.687-55A=	XP_016883624.1:n.687-55A=
XM_017028136.1:c.585-55A=	XP_016883625.1:n.585-55A=
NM_001250.6:c.647-50A= MANE Select	NP_001241.1:n.647-50A=
NM_001302753.2:c.687-50A=	NP_001289682.1:n.687-50A=
NM_001322421.2:c.658+44A=	NP_001309350.1:n.658+44A=
NM_001322422.2:c.491-50A=	NP_001309351.1:n.491-50A=
NM_001362758.2:c.647-55A=	NP_001349687.1:n.647-55A=
NM_152854.4:c.585-50A=	NP_690593.1:n.585-50A=
NR_126502.2:n.680-50A=
NR_136327.2:n.583-50A=