Canonical Allele Identifier: CA2366533720

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128897C= , CM000682.2:g.46128897C=	GRCh38
NC_000020.10:g.44757536C= , CM000682.1:g.44757536C=	GRCh37
NC_000020.9:g.44190943C=	NCBI36
NG_007279.1:g.15631C= , LRG_40:g.15631C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.693C=	ENSP00000512095.1:n.693C=
ENST00000489304.6:c.774C=	ENSP00000512096.1:n.774C=
ENST00000695675.1:n.2567C=
ENST00000372285.8:c.691C= MANE Select	ENSP00000361359.3:p.Gln231=
ENST00000372276.7:c.*17C=	ENSP00000361350.3:n.*17C=
ENST00000372285.7:c.691C=	ENSP00000361359.3:p.Gln231=
ENST00000466205.5:c.593C=
ENST00000477696.5:n.664C=
ENST00000489304.5:n.767C=
ENST00000620709.4:c.*238C=	ENSP00000484074.1:n.*238C=
NM_001250.5:c.691C=	NP_001241.1:p.Gln231=
NM_001302753.1:c.*17C=	NP_001289682.1:n.*17C=
NM_152854.3:c.*17C=	NP_690593.1:n.*17C=
NR_126502.1:n.784C=
XM_005260617.2:c.703C=	XP_005260674.1:p.Gln235=
XM_005260619.2:c.547C=	XP_005260676.1:p.Gln183=
XR_936660.1:n.691C=
NM_001322421.1:c.703C=	NP_001309350.1:p.Gln235=
NM_001322422.1:c.535C=	NP_001309351.1:p.Gln179=
NM_001362758.1:c.*17C=	NP_001349687.1:n.*17C=
NR_136327.1:n.687C=
XM_005260619.3:c.547C=	XP_005260676.1:p.Gln183=
XM_017028135.1:c.726C=	XP_016883624.1:p.Ser242=
XM_017028136.1:c.624C=	XP_016883625.1:p.Ser208=
NM_001250.6:c.691C= MANE Select	NP_001241.1:p.Gln231=
NM_001302753.2:c.*17C=	NP_001289682.1:n.*17C=
NM_001322421.2:c.703C=	NP_001309350.1:p.Gln235=
NM_001322422.2:c.535C=	NP_001309351.1:p.Gln179=
NM_001362758.2:c.*17C=	NP_001349687.1:n.*17C=
NM_152854.4:c.*17C=	NP_690593.1:n.*17C=
NR_126502.2:n.724C=
NR_136327.2:n.627C=