Canonical Allele Identifier: CA2366533225

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129104C= , CM000682.2:g.46129104C=	GRCh38
NC_000020.10:g.44757743C= , CM000682.1:g.44757743C=	GRCh37
NC_000020.9:g.44191150C=	NCBI36
NG_007279.1:g.15838C= , LRG_40:g.15838C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.981C=	ENSP00000512096.1:n.981C=
ENST00000695675.1:n.2774C=
ENST00000372285.8:c.*64C= MANE Select	ENSP00000361359.3:n.*64C=
ENST00000372276.7:c.*224C=	ENSP00000361350.3:n.*224C=
ENST00000372285.7:c.*64C=	ENSP00000361359.3:n.*64C=
ENST00000466205.5:c.800C=
ENST00000489304.5:n.974C=
ENST00000620709.4:c.*445C=	ENSP00000484074.1:n.*445C=
NM_001250.5:c.*64C=	NP_001241.1:n.*64C=
NM_001302753.1:c.*224C=	NP_001289682.1:n.*224C=
NM_152854.3:c.*224C=	NP_690593.1:n.*224C=
NR_126502.1:n.991C=
XM_005260617.2:c.*64C=	XP_005260674.1:n.*64C=
XM_005260619.2:c.*64C=	XP_005260676.1:n.*64C=
NM_001322421.1:c.*64C=	NP_001309350.1:n.*64C=
NM_001322422.1:c.*64C=	NP_001309351.1:n.*64C=
NM_001362758.1:c.*224C=	NP_001349687.1:n.*224C=
NR_136327.1:n.894C=
XM_005260619.3:c.*64C=	XP_005260676.1:n.*64C=
XM_017028135.1:c.933C=	XP_016883624.1:p.Cys311=
XM_017028136.1:c.831C=	XP_016883625.1:p.Cys277=
NM_001250.6:c.*64C= MANE Select	NP_001241.1:n.*64C=
NM_001302753.2:c.*224C=	NP_001289682.1:n.*224C=
NM_001322421.2:c.*64C=	NP_001309350.1:n.*64C=
NM_001322422.2:c.*64C=	NP_001309351.1:n.*64C=
NM_001362758.2:c.*224C=	NP_001349687.1:n.*224C=
NM_152854.4:c.*224C=	NP_690593.1:n.*224C=
NR_126502.2:n.931C=
NR_136327.2:n.834C=