Canonical Allele Identifier: CA2366533238

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129125G= , CM000682.2:g.46129125G=	GRCh38
NC_000020.10:g.44757764G= , CM000682.1:g.44757764G=	GRCh37
NC_000020.9:g.44191171G=	NCBI36
NG_007279.1:g.15859G= , LRG_40:g.15859G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1002G=	ENSP00000512096.1:n.1002G=
ENST00000695675.1:n.2795G=
ENST00000372285.8:c.*85G= MANE Select	ENSP00000361359.3:n.*85G=
ENST00000372276.7:c.*245G=	ENSP00000361350.3:n.*245G=
ENST00000372285.7:c.*85G=	ENSP00000361359.3:n.*85G=
ENST00000466205.5:c.821G=
ENST00000489304.5:n.995G=
ENST00000620709.4:c.*466G=	ENSP00000484074.1:n.*466G=
NM_001250.5:c.*85G=	NP_001241.1:n.*85G=
NM_001302753.1:c.*245G=	NP_001289682.1:n.*245G=
NM_152854.3:c.*245G=	NP_690593.1:n.*245G=
NR_126502.1:n.1012G=
XM_005260617.2:c.*85G=	XP_005260674.1:n.*85G=
XM_005260619.2:c.*85G=	XP_005260676.1:n.*85G=
NM_001322421.1:c.*85G=	NP_001309350.1:n.*85G=
NM_001322422.1:c.*85G=	NP_001309351.1:n.*85G=
NM_001362758.1:c.*245G=	NP_001349687.1:n.*245G=
NR_136327.1:n.915G=
XM_005260619.3:c.*85G=	XP_005260676.1:n.*85G=
XM_017028135.1:c.954G=	XP_016883624.1:p.Arg318=
XM_017028136.1:c.852G=	XP_016883625.1:p.Arg284=
NM_001250.6:c.*85G= MANE Select	NP_001241.1:n.*85G=
NM_001302753.2:c.*245G=	NP_001289682.1:n.*245G=
NM_001322421.2:c.*85G=	NP_001309350.1:n.*85G=
NM_001322422.2:c.*85G=	NP_001309351.1:n.*85G=
NM_001362758.2:c.*245G=	NP_001349687.1:n.*245G=
NM_152854.4:c.*245G=	NP_690593.1:n.*245G=
NR_126502.2:n.952G=
NR_136327.2:n.855G=