Canonical Allele Identifier: CA2739725301

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129051A>T , CM000682.2:g.46129051A>T	GRCh38
NC_000020.10:g.44757690A>T , CM000682.1:g.44757690A>T	GRCh37
NC_000020.9:g.44191097A>T	NCBI36
NG_007279.1:g.15785A>T , LRG_40:g.15785A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.928A>T	ENSP00000512096.1:n.928A>T
ENST00000695675.1:n.2721A>T
ENST00000372285.8:c.*11A>T MANE Select	ENSP00000361359.3:n.*11A>T
ENST00000372276.7:c.*171A>T	ENSP00000361350.3:n.*171A>T
ENST00000372285.7:c.*11A>T	ENSP00000361359.3:n.*11A>T
ENST00000466205.5:c.747A>T
ENST00000489304.5:n.921A>T
ENST00000620709.4:c.*392A>T	ENSP00000484074.1:n.*392A>T
NM_001250.5:c.*11A>T	NP_001241.1:n.*11A>T
NM_001302753.1:c.*171A>T	NP_001289682.1:n.*171A>T
NM_152854.3:c.*171A>T	NP_690593.1:n.*171A>T
NR_126502.1:n.938A>T
XM_005260617.2:c.*11A>T	XP_005260674.1:n.*11A>T
XM_005260619.2:c.*11A>T	XP_005260676.1:n.*11A>T
NM_001322421.1:c.*11A>T	NP_001309350.1:n.*11A>T
NM_001322422.1:c.*11A>T	NP_001309351.1:n.*11A>T
NM_001362758.1:c.*171A>T	NP_001349687.1:n.*171A>T
NR_136327.1:n.841A>T
XM_005260619.3:c.*11A>T	XP_005260676.1:n.*11A>T
XM_017028135.1:c.880A>T	XP_016883624.1:p.Thr294Ser
XM_017028136.1:c.778A>T	XP_016883625.1:p.Thr260Ser
NM_001250.6:c.*11A>T MANE Select	NP_001241.1:n.*11A>T
NM_001302753.2:c.*171A>T	NP_001289682.1:n.*171A>T
NM_001322421.2:c.*11A>T	NP_001309350.1:n.*11A>T
NM_001322422.2:c.*11A>T	NP_001309351.1:n.*11A>T
NM_001362758.2:c.*171A>T	NP_001349687.1:n.*171A>T
NM_152854.4:c.*171A>T	NP_690593.1:n.*171A>T
NR_126502.2:n.878A>T
NR_136327.2:n.781A>T