Canonical Allele Identifier: CA2366533202

Gene: CD40

Linked Data

• dbSNP Id: rs762015042

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129060T>G , CM000682.2:g.46129060T>G	GRCh38
NC_000020.10:g.44757699T>G , CM000682.1:g.44757699T>G	GRCh37
NC_000020.9:g.44191106T>G	NCBI36
NG_007279.1:g.15794T>G , LRG_40:g.15794T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.937T>G	ENSP00000512096.1:n.937T>G
ENST00000695675.1:n.2730T>G
ENST00000372285.8:c.*20T>G MANE Select	ENSP00000361359.3:n.*20T>G
ENST00000372276.7:c.*180T>G	ENSP00000361350.3:n.*180T>G
ENST00000372285.7:c.*20T>G	ENSP00000361359.3:n.*20T>G
ENST00000466205.5:c.756T>G
ENST00000489304.5:n.930T>G
ENST00000620709.4:c.*401T>G	ENSP00000484074.1:n.*401T>G
NM_001250.5:c.*20T>G	NP_001241.1:n.*20T>G
NM_001302753.1:c.*180T>G	NP_001289682.1:n.*180T>G
NM_152854.3:c.*180T>G	NP_690593.1:n.*180T>G
NR_126502.1:n.947T>G
XM_005260617.2:c.*20T>G	XP_005260674.1:n.*20T>G
XM_005260619.2:c.*20T>G	XP_005260676.1:n.*20T>G
NM_001322421.1:c.*20T>G	NP_001309350.1:n.*20T>G
NM_001322422.1:c.*20T>G	NP_001309351.1:n.*20T>G
NM_001362758.1:c.*180T>G	NP_001349687.1:n.*180T>G
NR_136327.1:n.850T>G
XM_005260619.3:c.*20T>G	XP_005260676.1:n.*20T>G
XM_017028135.1:c.889T>G	XP_016883624.1:p.Cys297Gly
XM_017028136.1:c.787T>G	XP_016883625.1:p.Cys263Gly
NM_001250.6:c.*20T>G MANE Select	NP_001241.1:n.*20T>G
NM_001302753.2:c.*180T>G	NP_001289682.1:n.*180T>G
NM_001322421.2:c.*20T>G	NP_001309350.1:n.*20T>G
NM_001322422.2:c.*20T>G	NP_001309351.1:n.*20T>G
NM_001362758.2:c.*180T>G	NP_001349687.1:n.*180T>G
NM_152854.4:c.*180T>G	NP_690593.1:n.*180T>G
NR_126502.2:n.887T>G
NR_136327.2:n.790T>G