Canonical Allele Identifier: CA409212328

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757657T>A (hg19) ; chr20:g.46129018T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129018T>A , CM000682.2:g.46129018T>A	GRCh38
NC_000020.10:g.44757657T>A , CM000682.1:g.44757657T>A	GRCh37
NC_000020.9:g.44191064T>A	NCBI36
NG_007279.1:g.15752T>A , LRG_40:g.15752T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.895T>A	ENSP00000512096.1:n.895T>A
ENST00000695675.1:n.2688T>A
ENST00000372285.8:c.812T>A MANE Select	ENSP00000361359.3:p.Ile271Asn
ENST00000372276.7:c.*138T>A	ENSP00000361350.3:n.*138T>A
ENST00000372285.7:c.812T>A	ENSP00000361359.3:p.Ile271Asn
ENST00000466205.5:c.714T>A
ENST00000489304.5:n.888T>A
ENST00000620709.4:c.*359T>A	ENSP00000484074.1:n.*359T>A
NM_001250.5:c.812T>A	NP_001241.1:p.Ile271Asn
NM_001302753.1:c.*138T>A	NP_001289682.1:n.*138T>A
NM_152854.3:c.*138T>A	NP_690593.1:n.*138T>A
NR_126502.1:n.905T>A
XM_005260617.2:c.824T>A	XP_005260674.1:p.Ile275Asn
XM_005260619.2:c.668T>A	XP_005260676.1:p.Ile223Asn
XR_936660.1:n.812T>A
NM_001322421.1:c.824T>A	NP_001309350.1:p.Ile275Asn
NM_001322422.1:c.656T>A	NP_001309351.1:p.Ile219Asn
NM_001362758.1:c.*138T>A	NP_001349687.1:n.*138T>A
NR_136327.1:n.808T>A
XM_005260619.3:c.668T>A	XP_005260676.1:p.Ile223Asn
XM_017028135.1:c.847T>A	XP_016883624.1:p.Ser283Thr
XM_017028136.1:c.745T>A	XP_016883625.1:p.Ser249Thr
NM_001250.6:c.812T>A MANE Select	NP_001241.1:p.Ile271Asn
NM_001302753.2:c.*138T>A	NP_001289682.1:n.*138T>A
NM_001322421.2:c.824T>A	NP_001309350.1:p.Ile275Asn
NM_001322422.2:c.656T>A	NP_001309351.1:p.Ile219Asn
NM_001362758.2:c.*138T>A	NP_001349687.1:n.*138T>A
NM_152854.4:c.*138T>A	NP_690593.1:n.*138T>A
NR_126502.2:n.845T>A
NR_136327.2:n.748T>A