Canonical Allele Identifier: CA2366533716

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128887C= , CM000682.2:g.46128887C=	GRCh38
NC_000020.10:g.44757526C= , CM000682.1:g.44757526C=	GRCh37
NC_000020.9:g.44190933C=	NCBI36
NG_007279.1:g.15621C= , LRG_40:g.15621C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.683C=	ENSP00000512095.1:n.683C=
ENST00000489304.6:c.764C=	ENSP00000512096.1:n.764C=
ENST00000695675.1:n.2557C=
ENST00000372285.8:c.681C= MANE Select	ENSP00000361359.3:p.Pro227=
ENST00000372276.7:c.*7C=	ENSP00000361350.3:n.*7C=
ENST00000372285.7:c.681C=	ENSP00000361359.3:p.Pro227=
ENST00000466205.5:c.583C=
ENST00000477696.5:n.654C=
ENST00000489304.5:n.757C=
ENST00000620709.4:c.*228C=	ENSP00000484074.1:n.*228C=
NM_001250.5:c.681C=	NP_001241.1:p.Pro227=
NM_001302753.1:c.*7C=	NP_001289682.1:n.*7C=
NM_152854.3:c.*7C=	NP_690593.1:n.*7C=
NR_126502.1:n.774C=
XM_005260617.2:c.693C=	XP_005260674.1:p.Pro231=
XM_005260619.2:c.537C=	XP_005260676.1:p.Pro179=
XR_936660.1:n.681C=
NM_001322421.1:c.693C=	NP_001309350.1:p.Pro231=
NM_001322422.1:c.525C=	NP_001309351.1:p.Pro175=
NM_001362758.1:c.*7C=	NP_001349687.1:n.*7C=
NR_136327.1:n.677C=
XM_005260619.3:c.537C=	XP_005260676.1:p.Pro179=
XM_017028135.1:c.716C=	XP_016883624.1:p.Pro239=
XM_017028136.1:c.614C=	XP_016883625.1:p.Pro205=
NM_001250.6:c.681C= MANE Select	NP_001241.1:p.Pro227=
NM_001302753.2:c.*7C=	NP_001289682.1:n.*7C=
NM_001322421.2:c.693C=	NP_001309350.1:p.Pro231=
NM_001322422.2:c.525C=	NP_001309351.1:p.Pro175=
NM_001362758.2:c.*7C=	NP_001349687.1:n.*7C=
NM_152854.4:c.*7C=	NP_690593.1:n.*7C=
NR_126502.2:n.714C=
NR_136327.2:n.617C=