Canonical Allele Identifier: CA2366533290

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129192G= , CM000682.2:g.46129192G=	GRCh38
NC_000020.10:g.44757831G= , CM000682.1:g.44757831G=	GRCh37
NC_000020.9:g.44191238G=	NCBI36
NG_007279.1:g.15926G= , LRG_40:g.15926G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1069G=	ENSP00000512096.1:n.1069G=
ENST00000695675.1:n.2862G=
ENST00000372285.8:c.*152G= MANE Select	ENSP00000361359.3:n.*152G=
ENST00000372276.7:c.*312G=	ENSP00000361350.3:n.*312G=
ENST00000372285.7:c.*152G=	ENSP00000361359.3:n.*152G=
ENST00000489304.5:n.1062G=
ENST00000620709.4:c.*533G=	ENSP00000484074.1:n.*533G=
NM_001250.5:c.*152G=	NP_001241.1:n.*152G=
NM_001302753.1:c.*312G=	NP_001289682.1:n.*312G=
NM_152854.3:c.*312G=	NP_690593.1:n.*312G=
NR_126502.1:n.1079G=
XM_005260617.2:c.*152G=	XP_005260674.1:n.*152G=
XM_005260619.2:c.*152G=	XP_005260676.1:n.*152G=
NM_001322421.1:c.*152G=	NP_001309350.1:n.*152G=
NM_001322422.1:c.*152G=	NP_001309351.1:n.*152G=
NM_001362758.1:c.*312G=	NP_001349687.1:n.*312G=
NR_136327.1:n.982G=
XM_005260619.3:c.*152G=	XP_005260676.1:n.*152G=
XM_017028135.1:c.*49G=	XP_016883624.1:n.*49G=
XM_017028136.1:c.*49G=	XP_016883625.1:n.*49G=
NM_001250.6:c.*152G= MANE Select	NP_001241.1:n.*152G=
NM_001302753.2:c.*312G=	NP_001289682.1:n.*312G=
NM_001322421.2:c.*152G=	NP_001309350.1:n.*152G=
NM_001322422.2:c.*152G=	NP_001309351.1:n.*152G=
NM_001362758.2:c.*312G=	NP_001349687.1:n.*312G=
NM_152854.4:c.*312G=	NP_690593.1:n.*312G=
NR_126502.2:n.1019G=
NR_136327.2:n.922G=