Canonical Allele Identifier: CA2739725314

Gene: CD40

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129058A>T , CM000682.2:g.46129058A>T	GRCh38
NC_000020.10:g.44757697A>T , CM000682.1:g.44757697A>T	GRCh37
NC_000020.9:g.44191104A>T	NCBI36
NG_007279.1:g.15792A>T , LRG_40:g.15792A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.935A>T	ENSP00000512096.1:n.935A>T
ENST00000695675.1:n.2728A>T
ENST00000372285.8:c.*18A>T MANE Select	ENSP00000361359.3:n.*18A>T
ENST00000372276.7:c.*178A>T	ENSP00000361350.3:n.*178A>T
ENST00000372285.7:c.*18A>T	ENSP00000361359.3:n.*18A>T
ENST00000466205.5:c.754A>T
ENST00000489304.5:n.928A>T
ENST00000620709.4:c.*399A>T	ENSP00000484074.1:n.*399A>T
NM_001250.5:c.*18A>T	NP_001241.1:n.*18A>T
NM_001302753.1:c.*178A>T	NP_001289682.1:n.*178A>T
NM_152854.3:c.*178A>T	NP_690593.1:n.*178A>T
NR_126502.1:n.945A>T
XM_005260617.2:c.*18A>T	XP_005260674.1:n.*18A>T
XM_005260619.2:c.*18A>T	XP_005260676.1:n.*18A>T
NM_001322421.1:c.*18A>T	NP_001309350.1:n.*18A>T
NM_001322422.1:c.*18A>T	NP_001309351.1:n.*18A>T
NM_001362758.1:c.*178A>T	NP_001349687.1:n.*178A>T
NR_136327.1:n.848A>T
XM_005260619.3:c.*18A>T	XP_005260676.1:n.*18A>T
XM_017028135.1:c.887A>T	XP_016883624.1:p.Glu296Val
XM_017028136.1:c.785A>T	XP_016883625.1:p.Glu262Val
NM_001250.6:c.*18A>T MANE Select	NP_001241.1:n.*18A>T
NM_001302753.2:c.*178A>T	NP_001289682.1:n.*178A>T
NM_001322421.2:c.*18A>T	NP_001309350.1:n.*18A>T
NM_001322422.2:c.*18A>T	NP_001309351.1:n.*18A>T
NM_001362758.2:c.*178A>T	NP_001349687.1:n.*178A>T
NM_152854.4:c.*178A>T	NP_690593.1:n.*178A>T
NR_126502.2:n.885A>T
NR_136327.2:n.788A>T