Canonical Allele Identifier: CA409211992

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757603A>T (hg19) ; chr20:g.46128964A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128964A>T , CM000682.2:g.46128964A>T	GRCh38
NC_000020.10:g.44757603A>T , CM000682.1:g.44757603A>T	GRCh37
NC_000020.9:g.44191010A>T	NCBI36
NG_007279.1:g.15698A>T , LRG_40:g.15698A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.760A>T	ENSP00000512095.1:n.760A>T
ENST00000489304.6:c.841A>T	ENSP00000512096.1:n.841A>T
ENST00000695675.1:n.2634A>T
ENST00000372285.8:c.758A>T MANE Select	ENSP00000361359.3:p.Glu253Val
ENST00000372276.7:c.*84A>T	ENSP00000361350.3:n.*84A>T
ENST00000372285.7:c.758A>T	ENSP00000361359.3:p.Glu253Val
ENST00000466205.5:c.660A>T
ENST00000477696.5:n.731A>T
ENST00000489304.5:n.834A>T
ENST00000620709.4:c.*305A>T	ENSP00000484074.1:n.*305A>T
NM_001250.5:c.758A>T	NP_001241.1:p.Glu253Val
NM_001302753.1:c.*84A>T	NP_001289682.1:n.*84A>T
NM_152854.3:c.*84A>T	NP_690593.1:n.*84A>T
NR_126502.1:n.851A>T
XM_005260617.2:c.770A>T	XP_005260674.1:p.Glu257Val
XM_005260619.2:c.614A>T	XP_005260676.1:p.Glu205Val
XR_936660.1:n.758A>T
NM_001322421.1:c.770A>T	NP_001309350.1:p.Glu257Val
NM_001322422.1:c.602A>T	NP_001309351.1:p.Glu201Val
NM_001362758.1:c.*84A>T	NP_001349687.1:n.*84A>T
NR_136327.1:n.754A>T
XM_005260619.3:c.614A>T	XP_005260676.1:p.Glu205Val
XM_017028135.1:c.793A>T	XP_016883624.1:p.Arg265Ter
XM_017028136.1:c.691A>T	XP_016883625.1:p.Arg231Ter
NM_001250.6:c.758A>T MANE Select	NP_001241.1:p.Glu253Val
NM_001302753.2:c.*84A>T	NP_001289682.1:n.*84A>T
NM_001322421.2:c.770A>T	NP_001309350.1:p.Glu257Val
NM_001322422.2:c.602A>T	NP_001309351.1:p.Glu201Val
NM_001362758.2:c.*84A>T	NP_001349687.1:n.*84A>T
NM_152854.4:c.*84A>T	NP_690593.1:n.*84A>T
NR_126502.2:n.791A>T
NR_136327.2:n.694A>T