Canonical Allele Identifier: CA409211534

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757531C>G (hg19) ; chr20:g.46128892C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128892C>G , CM000682.2:g.46128892C>G	GRCh38
NC_000020.10:g.44757531C>G , CM000682.1:g.44757531C>G	GRCh37
NC_000020.9:g.44190938C>G	NCBI36
NG_007279.1:g.15626C>G , LRG_40:g.15626C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.688C>G	ENSP00000512095.1:n.688C>G
ENST00000489304.6:c.769C>G	ENSP00000512096.1:n.769C>G
ENST00000695675.1:n.2562C>G
ENST00000372285.8:c.686C>G MANE Select	ENSP00000361359.3:p.Pro229Arg
ENST00000372276.7:c.*12C>G	ENSP00000361350.3:n.*12C>G
ENST00000372285.7:c.686C>G	ENSP00000361359.3:p.Pro229Arg
ENST00000466205.5:c.588C>G
ENST00000477696.5:n.659C>G
ENST00000489304.5:n.762C>G
ENST00000620709.4:c.*233C>G	ENSP00000484074.1:n.*233C>G
NM_001250.5:c.686C>G	NP_001241.1:p.Pro229Arg
NM_001302753.1:c.*12C>G	NP_001289682.1:n.*12C>G
NM_152854.3:c.*12C>G	NP_690593.1:n.*12C>G
NR_126502.1:n.779C>G
XM_005260617.2:c.698C>G	XP_005260674.1:p.Pro233Arg
XM_005260619.2:c.542C>G	XP_005260676.1:p.Pro181Arg
XR_936660.1:n.686C>G
NM_001322421.1:c.698C>G	NP_001309350.1:p.Pro233Arg
NM_001322422.1:c.530C>G	NP_001309351.1:p.Pro177Arg
NM_001362758.1:c.*12C>G	NP_001349687.1:n.*12C>G
NR_136327.1:n.682C>G
XM_005260619.3:c.542C>G	XP_005260676.1:p.Pro181Arg
XM_017028135.1:c.721C>G	XP_016883624.1:p.Pro241Ala
XM_017028136.1:c.619C>G	XP_016883625.1:p.Pro207Ala
NM_001250.6:c.686C>G MANE Select	NP_001241.1:p.Pro229Arg
NM_001302753.2:c.*12C>G	NP_001289682.1:n.*12C>G
NM_001322421.2:c.698C>G	NP_001309350.1:p.Pro233Arg
NM_001322422.2:c.530C>G	NP_001309351.1:p.Pro177Arg
NM_001362758.2:c.*12C>G	NP_001349687.1:n.*12C>G
NM_152854.4:c.*12C>G	NP_690593.1:n.*12C>G
NR_126502.2:n.719C>G
NR_136327.2:n.622C>G