Canonical Allele Identifier: CA409205676

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44751377T>G (hg19) ; chr20:g.46122738T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46122738T>G , CM000682.2:g.46122738T>G	GRCh38
NC_000020.10:g.44751377T>G , CM000682.1:g.44751377T>G	GRCh37
NC_000020.9:g.44184784T>G	NCBI36
NG_007279.1:g.9472T>G , LRG_40:g.9472T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.481T>G	ENSP00000512095.1:n.481T>G
ENST00000489304.6:c.385T>G	ENSP00000512096.1:p.Phe129Val
ENST00000695669.1:n.458T>G
ENST00000695670.1:n.365T>G
ENST00000695671.1:c.385T>G	ENSP00000512093.1:p.Phe129Val
ENST00000695672.1:n.310T>G
ENST00000695673.1:n.250T>G
ENST00000372285.8:c.385T>G MANE Select	ENSP00000361359.3:p.Phe129Val
ENST00000372276.7:c.385T>G	ENSP00000361350.3:p.Phe129Val
ENST00000372285.7:c.385T>G	ENSP00000361359.3:p.Phe129Val
ENST00000461171.1:n.170T>G
ENST00000466205.5:c.381T>G
ENST00000477696.5:n.452T>G
ENST00000489304.5:n.378T>G
ENST00000620709.4:c.385T>G	ENSP00000484074.1:p.Phe129Val
NM_001250.5:c.385T>G	NP_001241.1:p.Phe129Val
NM_001302753.1:c.385T>G	NP_001289682.1:p.Phe129Val
NM_152854.3:c.385T>G	NP_690593.1:p.Phe129Val
NR_126502.1:n.475T>G
XM_005260617.2:c.385T>G	XP_005260674.1:p.Phe129Val
XM_005260619.2:c.385T>G	XP_005260676.1:p.Phe129Val
XM_011529109.1:c.385T>G	XP_011527411.1:p.Phe129Val
XR_936660.1:n.479T>G
NM_001322421.1:c.385T>G	NP_001309350.1:p.Phe129Val
NM_001322422.1:c.385T>G	NP_001309351.1:p.Phe129Val
NM_001362758.1:c.385T>G	NP_001349687.1:p.Phe129Val
NR_136327.1:n.475T>G
XM_005260619.3:c.385T>G	XP_005260676.1:p.Phe129Val
XM_011529109.2:c.385T>G	XP_011527411.1:p.Phe129Val
XM_017028135.1:c.385T>G	XP_016883624.1:p.Phe129Val
XM_017028136.1:c.385T>G	XP_016883625.1:p.Phe129Val
NM_001250.6:c.385T>G MANE Select	NP_001241.1:p.Phe129Val
NM_001302753.2:c.385T>G	NP_001289682.1:p.Phe129Val
NM_001322421.2:c.385T>G	NP_001309350.1:p.Phe129Val
NM_001322422.2:c.385T>G	NP_001309351.1:p.Phe129Val
NM_001362758.2:c.385T>G	NP_001349687.1:p.Phe129Val
NM_152854.4:c.385T>G	NP_690593.1:p.Phe129Val
NR_126502.2:n.415T>G
NR_136327.2:n.415T>G