Canonical Allele Identifier: CA409211843

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757578T>A (hg19) ; chr20:g.46128939T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128939T>A , CM000682.2:g.46128939T>A	GRCh38
NC_000020.10:g.44757578T>A , CM000682.1:g.44757578T>A	GRCh37
NC_000020.9:g.44190985T>A	NCBI36
NG_007279.1:g.15673T>A , LRG_40:g.15673T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.735T>A	ENSP00000512095.1:n.735T>A
ENST00000489304.6:c.816T>A	ENSP00000512096.1:n.816T>A
ENST00000695675.1:n.2609T>A
ENST00000372285.8:c.733T>A MANE Select	ENSP00000361359.3:p.Ser245Thr
ENST00000372276.7:c.*59T>A	ENSP00000361350.3:n.*59T>A
ENST00000372285.7:c.733T>A	ENSP00000361359.3:p.Ser245Thr
ENST00000466205.5:c.635T>A
ENST00000477696.5:n.706T>A
ENST00000489304.5:n.809T>A
ENST00000620709.4:c.*280T>A	ENSP00000484074.1:n.*280T>A
NM_001250.5:c.733T>A	NP_001241.1:p.Ser245Thr
NM_001302753.1:c.*59T>A	NP_001289682.1:n.*59T>A
NM_152854.3:c.*59T>A	NP_690593.1:n.*59T>A
NR_126502.1:n.826T>A
XM_005260617.2:c.745T>A	XP_005260674.1:p.Ser249Thr
XM_005260619.2:c.589T>A	XP_005260676.1:p.Ser197Thr
XR_936660.1:n.733T>A
NM_001322421.1:c.745T>A	NP_001309350.1:p.Ser249Thr
NM_001322422.1:c.577T>A	NP_001309351.1:p.Ser193Thr
NM_001362758.1:c.*59T>A	NP_001349687.1:n.*59T>A
NR_136327.1:n.729T>A
XM_005260619.3:c.589T>A	XP_005260676.1:p.Ser197Thr
XM_017028135.1:c.768T>A	XP_016883624.1:p.Ala256=
XM_017028136.1:c.666T>A	XP_016883625.1:p.Ala222=
NM_001250.6:c.733T>A MANE Select	NP_001241.1:p.Ser245Thr
NM_001302753.2:c.*59T>A	NP_001289682.1:n.*59T>A
NM_001322421.2:c.745T>A	NP_001309350.1:p.Ser249Thr
NM_001322422.2:c.577T>A	NP_001309351.1:p.Ser193Thr
NM_001362758.2:c.*59T>A	NP_001349687.1:n.*59T>A
NM_152854.4:c.*59T>A	NP_690593.1:n.*59T>A
NR_126502.2:n.766T>A
NR_136327.2:n.669T>A