Canonical Allele Identifier: CA409209304

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44756834T>A (hg19) ; chr20:g.46128195T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128195T>A , CM000682.2:g.46128195T>A	GRCh38
NC_000020.10:g.44756834T>A , CM000682.1:g.44756834T>A	GRCh37
NC_000020.9:g.44190241T>A	NCBI36
NG_007279.1:g.14929T>A , LRG_40:g.14929T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.619T>A	ENSP00000512095.1:n.619T>A
ENST00000489304.6:c.700T>A	ENSP00000512096.1:n.700T>A
ENST00000695670.1:n.586T>A
ENST00000695671.1:c.657T>A	ENSP00000512093.1:p.Val219=
ENST00000695674.1:n.1096T>A
ENST00000695675.1:n.2493T>A
ENST00000372285.8:c.617T>A MANE Select	ENSP00000361359.3:p.Phe206Tyr
ENST00000372276.7:c.555T>A	ENSP00000361350.3:p.Val185=
ENST00000372285.7:c.617T>A	ENSP00000361359.3:p.Phe206Tyr
ENST00000466205.5:c.519T>A
ENST00000477696.5:n.590T>A
ENST00000489304.5:n.693T>A
ENST00000620709.4:c.*164T>A	ENSP00000484074.1:n.*164T>A
NM_001250.5:c.617T>A	NP_001241.1:p.Phe206Tyr
NM_001302753.1:c.657T>A	NP_001289682.1:p.Val219=
NM_152854.3:c.555T>A	NP_690593.1:p.Val185=
NR_126502.1:n.710T>A
XM_005260617.2:c.617T>A	XP_005260674.1:p.Phe206Tyr
XM_005260619.2:c.461T>A	XP_005260676.1:p.Phe154Tyr
XR_936660.1:n.617T>A
NM_001322421.1:c.617T>A	NP_001309350.1:p.Phe206Tyr
NM_001322422.1:c.461T>A	NP_001309351.1:p.Phe154Tyr
NM_001362758.1:c.617T>A	NP_001349687.1:p.Phe206Tyr
NR_136327.1:n.613T>A
XM_005260619.3:c.461T>A	XP_005260676.1:p.Phe154Tyr
XM_017028135.1:c.657T>A	XP_016883624.1:p.Val219=
XM_017028136.1:c.555T>A	XP_016883625.1:p.Val185=
NM_001250.6:c.617T>A MANE Select	NP_001241.1:p.Phe206Tyr
NM_001302753.2:c.657T>A	NP_001289682.1:p.Val219=
NM_001322421.2:c.617T>A	NP_001309350.1:p.Phe206Tyr
NM_001322422.2:c.461T>A	NP_001309351.1:p.Phe154Tyr
NM_001362758.2:c.617T>A	NP_001349687.1:p.Phe206Tyr
NM_152854.4:c.555T>A	NP_690593.1:p.Val185=
NR_126502.2:n.650T>A
NR_136327.2:n.553T>A