Canonical Allele Identifier: CA2366533265

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129167C= , CM000682.2:g.46129167C=	GRCh38
NC_000020.10:g.44757806C= , CM000682.1:g.44757806C=	GRCh37
NC_000020.9:g.44191213C=	NCBI36
NG_007279.1:g.15901C= , LRG_40:g.15901C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1044C=	ENSP00000512096.1:n.1044C=
ENST00000695675.1:n.2837C=
ENST00000372285.8:c.*127C= MANE Select	ENSP00000361359.3:n.*127C=
ENST00000372276.7:c.*287C=	ENSP00000361350.3:n.*287C=
ENST00000372285.7:c.*127C=	ENSP00000361359.3:n.*127C=
ENST00000489304.5:n.1037C=
ENST00000620709.4:c.*508C=	ENSP00000484074.1:n.*508C=
NM_001250.5:c.*127C=	NP_001241.1:n.*127C=
NM_001302753.1:c.*287C=	NP_001289682.1:n.*287C=
NM_152854.3:c.*287C=	NP_690593.1:n.*287C=
NR_126502.1:n.1054C=
XM_005260617.2:c.*127C=	XP_005260674.1:n.*127C=
XM_005260619.2:c.*127C=	XP_005260676.1:n.*127C=
NM_001322421.1:c.*127C=	NP_001309350.1:n.*127C=
NM_001322422.1:c.*127C=	NP_001309351.1:n.*127C=
NM_001362758.1:c.*287C=	NP_001349687.1:n.*287C=
NR_136327.1:n.957C=
XM_005260619.3:c.*127C=	XP_005260676.1:n.*127C=
XM_017028135.1:c.*24C=	XP_016883624.1:n.*24C=
XM_017028136.1:c.*24C=	XP_016883625.1:n.*24C=
NM_001250.6:c.*127C= MANE Select	NP_001241.1:n.*127C=
NM_001302753.2:c.*287C=	NP_001289682.1:n.*287C=
NM_001322421.2:c.*127C=	NP_001309350.1:n.*127C=
NM_001322422.2:c.*127C=	NP_001309351.1:n.*127C=
NM_001362758.2:c.*287C=	NP_001349687.1:n.*287C=
NM_152854.4:c.*287C=	NP_690593.1:n.*287C=
NR_126502.2:n.994C=
NR_136327.2:n.897C=