Canonical Allele Identifier: CA2366533210

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129078C= , CM000682.2:g.46129078C=	GRCh38
NC_000020.10:g.44757717C= , CM000682.1:g.44757717C=	GRCh37
NC_000020.9:g.44191124C=	NCBI36
NG_007279.1:g.15812C= , LRG_40:g.15812C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.955C=	ENSP00000512096.1:n.955C=
ENST00000695675.1:n.2748C=
ENST00000372285.8:c.*38C= MANE Select	ENSP00000361359.3:n.*38C=
ENST00000372276.7:c.*198C=	ENSP00000361350.3:n.*198C=
ENST00000372285.7:c.*38C=	ENSP00000361359.3:n.*38C=
ENST00000466205.5:c.774C=
ENST00000489304.5:n.948C=
ENST00000620709.4:c.*419C=	ENSP00000484074.1:n.*419C=
NM_001250.5:c.*38C=	NP_001241.1:n.*38C=
NM_001302753.1:c.*198C=	NP_001289682.1:n.*198C=
NM_152854.3:c.*198C=	NP_690593.1:n.*198C=
NR_126502.1:n.965C=
XM_005260617.2:c.*38C=	XP_005260674.1:n.*38C=
XM_005260619.2:c.*38C=	XP_005260676.1:n.*38C=
NM_001322421.1:c.*38C=	NP_001309350.1:n.*38C=
NM_001322422.1:c.*38C=	NP_001309351.1:n.*38C=
NM_001362758.1:c.*198C=	NP_001349687.1:n.*198C=
NR_136327.1:n.868C=
XM_005260619.3:c.*38C=	XP_005260676.1:n.*38C=
XM_017028135.1:c.907C=	XP_016883624.1:p.Gln303=
XM_017028136.1:c.805C=	XP_016883625.1:p.Gln269=
NM_001250.6:c.*38C= MANE Select	NP_001241.1:n.*38C=
NM_001302753.2:c.*198C=	NP_001289682.1:n.*198C=
NM_001322421.2:c.*38C=	NP_001309350.1:n.*38C=
NM_001322422.2:c.*38C=	NP_001309351.1:n.*38C=
NM_001362758.2:c.*198C=	NP_001349687.1:n.*198C=
NM_152854.4:c.*198C=	NP_690593.1:n.*198C=
NR_126502.2:n.905C=
NR_136327.2:n.808C=