Canonical Allele Identifier: CA2366533306

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129209G= , CM000682.2:g.46129209G=	GRCh38
NC_000020.10:g.44757848G= , CM000682.1:g.44757848G=	GRCh37
NC_000020.9:g.44191255G=	NCBI36
NG_007279.1:g.15943G= , LRG_40:g.15943G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1086G=	ENSP00000512096.1:n.1086G=
ENST00000695675.1:n.2879G=
ENST00000372285.8:c.*169G= MANE Select	ENSP00000361359.3:n.*169G=
ENST00000372276.7:c.*329G=	ENSP00000361350.3:n.*329G=
ENST00000372285.7:c.*169G=	ENSP00000361359.3:n.*169G=
ENST00000489304.5:n.1079G=
ENST00000620709.4:c.*550G=	ENSP00000484074.1:n.*550G=
NM_001250.5:c.*169G=	NP_001241.1:n.*169G=
NM_001302753.1:c.*329G=	NP_001289682.1:n.*329G=
NM_152854.3:c.*329G=	NP_690593.1:n.*329G=
NR_126502.1:n.1096G=
XM_005260617.2:c.*169G=	XP_005260674.1:n.*169G=
XM_005260619.2:c.*169G=	XP_005260676.1:n.*169G=
NM_001322421.1:c.*169G=	NP_001309350.1:n.*169G=
NM_001322422.1:c.*169G=	NP_001309351.1:n.*169G=
NM_001362758.1:c.*329G=	NP_001349687.1:n.*329G=
NR_136327.1:n.999G=
XM_005260619.3:c.*169G=	XP_005260676.1:n.*169G=
XM_017028135.1:c.*66G=	XP_016883624.1:n.*66G=
XM_017028136.1:c.*66G=	XP_016883625.1:n.*66G=
NM_001250.6:c.*169G= MANE Select	NP_001241.1:n.*169G=
NM_001302753.2:c.*329G=	NP_001289682.1:n.*329G=
NM_001322421.2:c.*169G=	NP_001309350.1:n.*169G=
NM_001322422.2:c.*169G=	NP_001309351.1:n.*169G=
NM_001362758.2:c.*329G=	NP_001349687.1:n.*329G=
NM_152854.4:c.*329G=	NP_690593.1:n.*329G=
NR_126502.2:n.1036G=
NR_136327.2:n.939G=