Canonical Allele Identifier: CA409211733

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757558T>G (hg19) ; chr20:g.46128919T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128919T>G , CM000682.2:g.46128919T>G	GRCh38
NC_000020.10:g.44757558T>G , CM000682.1:g.44757558T>G	GRCh37
NC_000020.9:g.44190965T>G	NCBI36
NG_007279.1:g.15653T>G , LRG_40:g.15653T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.715T>G	ENSP00000512095.1:n.715T>G
ENST00000489304.6:c.796T>G	ENSP00000512096.1:n.796T>G
ENST00000695675.1:n.2589T>G
ENST00000372285.8:c.713T>G MANE Select	ENSP00000361359.3:p.Phe238Cys
ENST00000372276.7:c.*39T>G	ENSP00000361350.3:n.*39T>G
ENST00000372285.7:c.713T>G	ENSP00000361359.3:p.Phe238Cys
ENST00000466205.5:c.615T>G
ENST00000477696.5:n.686T>G
ENST00000489304.5:n.789T>G
ENST00000620709.4:c.*260T>G	ENSP00000484074.1:n.*260T>G
NM_001250.5:c.713T>G	NP_001241.1:p.Phe238Cys
NM_001302753.1:c.*39T>G	NP_001289682.1:n.*39T>G
NM_152854.3:c.*39T>G	NP_690593.1:n.*39T>G
NR_126502.1:n.806T>G
XM_005260617.2:c.725T>G	XP_005260674.1:p.Phe242Cys
XM_005260619.2:c.569T>G	XP_005260676.1:p.Phe190Cys
XR_936660.1:n.713T>G
NM_001322421.1:c.725T>G	NP_001309350.1:p.Phe242Cys
NM_001322422.1:c.557T>G	NP_001309351.1:p.Phe186Cys
NM_001362758.1:c.*39T>G	NP_001349687.1:n.*39T>G
NR_136327.1:n.709T>G
XM_005260619.3:c.569T>G	XP_005260676.1:p.Phe190Cys
XM_017028135.1:c.748T>G	XP_016883624.1:p.Phe250Val
XM_017028136.1:c.646T>G	XP_016883625.1:p.Phe216Val
NM_001250.6:c.713T>G MANE Select	NP_001241.1:p.Phe238Cys
NM_001302753.2:c.*39T>G	NP_001289682.1:n.*39T>G
NM_001322421.2:c.725T>G	NP_001309350.1:p.Phe242Cys
NM_001322422.2:c.557T>G	NP_001309351.1:p.Phe186Cys
NM_001362758.2:c.*39T>G	NP_001349687.1:n.*39T>G
NM_152854.4:c.*39T>G	NP_690593.1:n.*39T>G
NR_126502.2:n.746T>G
NR_136327.2:n.649T>G