Canonical Allele Identifier: CA409212448

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757670G>C (hg19) ; chr20:g.46129031G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129031G>C , CM000682.2:g.46129031G>C	GRCh38
NC_000020.10:g.44757670G>C , CM000682.1:g.44757670G>C	GRCh37
NC_000020.9:g.44191077G>C	NCBI36
NG_007279.1:g.15765G>C , LRG_40:g.15765G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.908G>C	ENSP00000512096.1:n.908G>C
ENST00000695675.1:n.2701G>C
ENST00000372285.8:c.825G>C MANE Select	ENSP00000361359.3:p.Glu275Asp
ENST00000372276.7:c.*151G>C	ENSP00000361350.3:n.*151G>C
ENST00000372285.7:c.825G>C	ENSP00000361359.3:p.Glu275Asp
ENST00000466205.5:c.727G>C
ENST00000489304.5:n.901G>C
ENST00000620709.4:c.*372G>C	ENSP00000484074.1:n.*372G>C
NM_001250.5:c.825G>C	NP_001241.1:p.Glu275Asp
NM_001302753.1:c.*151G>C	NP_001289682.1:n.*151G>C
NM_152854.3:c.*151G>C	NP_690593.1:n.*151G>C
NR_126502.1:n.918G>C
XM_005260617.2:c.837G>C	XP_005260674.1:p.Glu279Asp
XM_005260619.2:c.681G>C	XP_005260676.1:p.Glu227Asp
XR_936660.1:n.825G>C
NM_001322421.1:c.837G>C	NP_001309350.1:p.Glu279Asp
NM_001322422.1:c.669G>C	NP_001309351.1:p.Glu223Asp
NM_001362758.1:c.*151G>C	NP_001349687.1:n.*151G>C
NR_136327.1:n.821G>C
XM_005260619.3:c.681G>C	XP_005260676.1:p.Glu227Asp
XM_017028135.1:c.860G>C	XP_016883624.1:p.Arg287Thr
XM_017028136.1:c.758G>C	XP_016883625.1:p.Arg253Thr
NM_001250.6:c.825G>C MANE Select	NP_001241.1:p.Glu275Asp
NM_001302753.2:c.*151G>C	NP_001289682.1:n.*151G>C
NM_001322421.2:c.837G>C	NP_001309350.1:p.Glu279Asp
NM_001322422.2:c.669G>C	NP_001309351.1:p.Glu223Asp
NM_001362758.2:c.*151G>C	NP_001349687.1:n.*151G>C
NM_152854.4:c.*151G>C	NP_690593.1:n.*151G>C
NR_126502.2:n.858G>C
NR_136327.2:n.761G>C