Canonical Allele Identifier: CA409209484

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44756849T>A (hg19) ; chr20:g.46128210T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128210T>A , CM000682.2:g.46128210T>A	GRCh38
NC_000020.10:g.44756849T>A , CM000682.1:g.44756849T>A	GRCh37
NC_000020.9:g.44190256T>A	NCBI36
NG_007279.1:g.14944T>A , LRG_40:g.14944T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.634T>A	ENSP00000512095.1:n.634T>A
ENST00000489304.6:c.715T>A	ENSP00000512096.1:n.715T>A
ENST00000695670.1:n.601T>A
ENST00000695671.1:c.672T>A	ENSP00000512093.1:p.Gly224=
ENST00000695674.1:n.1111T>A
ENST00000695675.1:n.2508T>A
ENST00000372285.8:c.632T>A MANE Select	ENSP00000361359.3:p.Val211Glu
ENST00000372276.7:c.570T>A	ENSP00000361350.3:p.Gly190=
ENST00000372285.7:c.632T>A	ENSP00000361359.3:p.Val211Glu
ENST00000466205.5:c.534T>A
ENST00000477696.5:n.605T>A
ENST00000489304.5:n.708T>A
ENST00000620709.4:c.*179T>A	ENSP00000484074.1:n.*179T>A
NM_001250.5:c.632T>A	NP_001241.1:p.Val211Glu
NM_001302753.1:c.672T>A	NP_001289682.1:p.Gly224=
NM_152854.3:c.570T>A	NP_690593.1:p.Gly190=
NR_126502.1:n.725T>A
XM_005260617.2:c.632T>A	XP_005260674.1:p.Val211Glu
XM_005260619.2:c.476T>A	XP_005260676.1:p.Val159Glu
XR_936660.1:n.632T>A
NM_001322421.1:c.632T>A	NP_001309350.1:p.Val211Glu
NM_001322422.1:c.476T>A	NP_001309351.1:p.Val159Glu
NM_001362758.1:c.632T>A	NP_001349687.1:p.Val211Glu
NR_136327.1:n.628T>A
XM_005260619.3:c.476T>A	XP_005260676.1:p.Val159Glu
XM_017028135.1:c.672T>A	XP_016883624.1:p.Gly224=
XM_017028136.1:c.570T>A	XP_016883625.1:p.Gly190=
NM_001250.6:c.632T>A MANE Select	NP_001241.1:p.Val211Glu
NM_001302753.2:c.672T>A	NP_001289682.1:p.Gly224=
NM_001322421.2:c.632T>A	NP_001309350.1:p.Val211Glu
NM_001322422.2:c.476T>A	NP_001309351.1:p.Val159Glu
NM_001362758.2:c.632T>A	NP_001349687.1:p.Val211Glu
NM_152854.4:c.570T>A	NP_690593.1:p.Gly190=
NR_126502.2:n.665T>A
NR_136327.2:n.568T>A