Canonical Allele Identifier: CA409212012

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757606C>A (hg19) ; chr20:g.46128967C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128967C>A , CM000682.2:g.46128967C>A	GRCh38
NC_000020.10:g.44757606C>A , CM000682.1:g.44757606C>A	GRCh37
NC_000020.9:g.44191013C>A	NCBI36
NG_007279.1:g.15701C>A , LRG_40:g.15701C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.763C>A	ENSP00000512095.1:n.763C>A
ENST00000489304.6:c.844C>A	ENSP00000512096.1:n.844C>A
ENST00000695675.1:n.2637C>A
ENST00000372285.8:c.761C>A MANE Select	ENSP00000361359.3:p.Thr254Asn
ENST00000372276.7:c.*87C>A	ENSP00000361350.3:n.*87C>A
ENST00000372285.7:c.761C>A	ENSP00000361359.3:p.Thr254Asn
ENST00000466205.5:c.663C>A
ENST00000477696.5:n.734C>A
ENST00000489304.5:n.837C>A
ENST00000620709.4:c.*308C>A	ENSP00000484074.1:n.*308C>A
NM_001250.5:c.761C>A	NP_001241.1:p.Thr254Asn
NM_001302753.1:c.*87C>A	NP_001289682.1:n.*87C>A
NM_152854.3:c.*87C>A	NP_690593.1:n.*87C>A
NR_126502.1:n.854C>A
XM_005260617.2:c.773C>A	XP_005260674.1:p.Thr258Asn
XM_005260619.2:c.617C>A	XP_005260676.1:p.Thr206Asn
XR_936660.1:n.761C>A
NM_001322421.1:c.773C>A	NP_001309350.1:p.Thr258Asn
NM_001322422.1:c.605C>A	NP_001309351.1:p.Thr202Asn
NM_001362758.1:c.*87C>A	NP_001349687.1:n.*87C>A
NR_136327.1:n.757C>A
XM_005260619.3:c.617C>A	XP_005260676.1:p.Thr206Asn
XM_017028135.1:c.796C>A	XP_016883624.1:p.Leu266Ile
XM_017028136.1:c.694C>A	XP_016883625.1:p.Leu232Ile
NM_001250.6:c.761C>A MANE Select	NP_001241.1:p.Thr254Asn
NM_001302753.2:c.*87C>A	NP_001289682.1:n.*87C>A
NM_001322421.2:c.773C>A	NP_001309350.1:p.Thr258Asn
NM_001322422.2:c.605C>A	NP_001309351.1:p.Thr202Asn
NM_001362758.2:c.*87C>A	NP_001349687.1:n.*87C>A
NM_152854.4:c.*87C>A	NP_690593.1:n.*87C>A
NR_126502.2:n.794C>A
NR_136327.2:n.697C>A