Canonical Allele Identifier: CA2366533194

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129026C= , CM000682.2:g.46129026C=	GRCh38
NC_000020.10:g.44757665C= , CM000682.1:g.44757665C=	GRCh37
NC_000020.9:g.44191072C=	NCBI36
NG_007279.1:g.15760C= , LRG_40:g.15760C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.903C=	ENSP00000512096.1:n.903C=
ENST00000695675.1:n.2696C=
ENST00000372285.8:c.820C= MANE Select	ENSP00000361359.3:p.Gln274=
ENST00000372276.7:c.*146C=	ENSP00000361350.3:n.*146C=
ENST00000372285.7:c.820C=	ENSP00000361359.3:p.Gln274=
ENST00000466205.5:c.722C=
ENST00000489304.5:n.896C=
ENST00000620709.4:c.*367C=	ENSP00000484074.1:n.*367C=
NM_001250.5:c.820C=	NP_001241.1:p.Gln274=
NM_001302753.1:c.*146C=	NP_001289682.1:n.*146C=
NM_152854.3:c.*146C=	NP_690593.1:n.*146C=
NR_126502.1:n.913C=
XM_005260617.2:c.832C=	XP_005260674.1:p.Gln278=
XM_005260619.2:c.676C=	XP_005260676.1:p.Gln226=
XR_936660.1:n.820C=
NM_001322421.1:c.832C=	NP_001309350.1:p.Gln278=
NM_001322422.1:c.664C=	NP_001309351.1:p.Gln222=
NM_001362758.1:c.*146C=	NP_001349687.1:n.*146C=
NR_136327.1:n.816C=
XM_005260619.3:c.676C=	XP_005260676.1:p.Gln226=
XM_017028135.1:c.855C=	XP_016883624.1:p.Cys285=
XM_017028136.1:c.753C=	XP_016883625.1:p.Cys251=
NM_001250.6:c.820C= MANE Select	NP_001241.1:p.Gln274=
NM_001302753.2:c.*146C=	NP_001289682.1:n.*146C=
NM_001322421.2:c.832C=	NP_001309350.1:p.Gln278=
NM_001322422.2:c.664C=	NP_001309351.1:p.Gln222=
NM_001362758.2:c.*146C=	NP_001349687.1:n.*146C=
NM_152854.4:c.*146C=	NP_690593.1:n.*146C=
NR_126502.2:n.853C=
NR_136327.2:n.756C=