Canonical Allele Identifier: CA409211564

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757536C>G (hg19) ; chr20:g.46128897C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128897C>G , CM000682.2:g.46128897C>G	GRCh38
NC_000020.10:g.44757536C>G , CM000682.1:g.44757536C>G	GRCh37
NC_000020.9:g.44190943C>G	NCBI36
NG_007279.1:g.15631C>G , LRG_40:g.15631C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.693C>G	ENSP00000512095.1:n.693C>G
ENST00000489304.6:c.774C>G	ENSP00000512096.1:n.774C>G
ENST00000695675.1:n.2567C>G
ENST00000372285.8:c.691C>G MANE Select	ENSP00000361359.3:p.Gln231Glu
ENST00000372276.7:c.*17C>G	ENSP00000361350.3:n.*17C>G
ENST00000372285.7:c.691C>G	ENSP00000361359.3:p.Gln231Glu
ENST00000466205.5:c.593C>G
ENST00000477696.5:n.664C>G
ENST00000489304.5:n.767C>G
ENST00000620709.4:c.*238C>G	ENSP00000484074.1:n.*238C>G
NM_001250.5:c.691C>G	NP_001241.1:p.Gln231Glu
NM_001302753.1:c.*17C>G	NP_001289682.1:n.*17C>G
NM_152854.3:c.*17C>G	NP_690593.1:n.*17C>G
NR_126502.1:n.784C>G
XM_005260617.2:c.703C>G	XP_005260674.1:p.Gln235Glu
XM_005260619.2:c.547C>G	XP_005260676.1:p.Gln183Glu
XR_936660.1:n.691C>G
NM_001322421.1:c.703C>G	NP_001309350.1:p.Gln235Glu
NM_001322422.1:c.535C>G	NP_001309351.1:p.Gln179Glu
NM_001362758.1:c.*17C>G	NP_001349687.1:n.*17C>G
NR_136327.1:n.687C>G
XM_005260619.3:c.547C>G	XP_005260676.1:p.Gln183Glu
XM_017028135.1:c.726C>G	XP_016883624.1:p.Ser242Arg
XM_017028136.1:c.624C>G	XP_016883625.1:p.Ser208Arg
NM_001250.6:c.691C>G MANE Select	NP_001241.1:p.Gln231Glu
NM_001302753.2:c.*17C>G	NP_001289682.1:n.*17C>G
NM_001322421.2:c.703C>G	NP_001309350.1:p.Gln235Glu
NM_001322422.2:c.535C>G	NP_001309351.1:p.Gln179Glu
NM_001362758.2:c.*17C>G	NP_001349687.1:n.*17C>G
NM_152854.4:c.*17C>G	NP_690593.1:n.*17C>G
NR_126502.2:n.724C>G
NR_136327.2:n.627C>G