Canonical Allele Identifier: CA2739725347

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129079A>T , CM000682.2:g.46129079A>T	GRCh38
NC_000020.10:g.44757718A>T , CM000682.1:g.44757718A>T	GRCh37
NC_000020.9:g.44191125A>T	NCBI36
NG_007279.1:g.15813A>T , LRG_40:g.15813A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.956A>T	ENSP00000512096.1:n.956A>T
ENST00000695675.1:n.2749A>T
ENST00000372285.8:c.*39A>T MANE Select	ENSP00000361359.3:n.*39A>T
ENST00000372276.7:c.*199A>T	ENSP00000361350.3:n.*199A>T
ENST00000372285.7:c.*39A>T	ENSP00000361359.3:n.*39A>T
ENST00000466205.5:c.775A>T
ENST00000489304.5:n.949A>T
ENST00000620709.4:c.*420A>T	ENSP00000484074.1:n.*420A>T
NM_001250.5:c.*39A>T	NP_001241.1:n.*39A>T
NM_001302753.1:c.*199A>T	NP_001289682.1:n.*199A>T
NM_152854.3:c.*199A>T	NP_690593.1:n.*199A>T
NR_126502.1:n.966A>T
XM_005260617.2:c.*39A>T	XP_005260674.1:n.*39A>T
XM_005260619.2:c.*39A>T	XP_005260676.1:n.*39A>T
NM_001322421.1:c.*39A>T	NP_001309350.1:n.*39A>T
NM_001322422.1:c.*39A>T	NP_001309351.1:n.*39A>T
NM_001362758.1:c.*199A>T	NP_001349687.1:n.*199A>T
NR_136327.1:n.869A>T
XM_005260619.3:c.*39A>T	XP_005260676.1:n.*39A>T
XM_017028135.1:c.908A>T	XP_016883624.1:p.Gln303Leu
XM_017028136.1:c.806A>T	XP_016883625.1:p.Gln269Leu
NM_001250.6:c.*39A>T MANE Select	NP_001241.1:n.*39A>T
NM_001302753.2:c.*199A>T	NP_001289682.1:n.*199A>T
NM_001322421.2:c.*39A>T	NP_001309350.1:n.*39A>T
NM_001322422.2:c.*39A>T	NP_001309351.1:n.*39A>T
NM_001362758.2:c.*199A>T	NP_001349687.1:n.*199A>T
NM_152854.4:c.*199A>T	NP_690593.1:n.*199A>T
NR_126502.2:n.906A>T
NR_136327.2:n.809A>T