Canonical Allele Identifier: CA409212195

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757636A>C (hg19) ; chr20:g.46128997A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128997A>C , CM000682.2:g.46128997A>C	GRCh38
NC_000020.10:g.44757636A>C , CM000682.1:g.44757636A>C	GRCh37
NC_000020.9:g.44191043A>C	NCBI36
NG_007279.1:g.15731A>C , LRG_40:g.15731A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.793A>C	ENSP00000512095.1:n.793A>C
ENST00000489304.6:c.874A>C	ENSP00000512096.1:n.874A>C
ENST00000695675.1:n.2667A>C
ENST00000372285.8:c.791A>C MANE Select	ENSP00000361359.3:p.Glu264Ala
ENST00000372276.7:c.*117A>C	ENSP00000361350.3:n.*117A>C
ENST00000372285.7:c.791A>C	ENSP00000361359.3:p.Glu264Ala
ENST00000466205.5:c.693A>C
ENST00000477696.5:n.764A>C
ENST00000489304.5:n.867A>C
ENST00000620709.4:c.*338A>C	ENSP00000484074.1:n.*338A>C
NM_001250.5:c.791A>C	NP_001241.1:p.Glu264Ala
NM_001302753.1:c.*117A>C	NP_001289682.1:n.*117A>C
NM_152854.3:c.*117A>C	NP_690593.1:n.*117A>C
NR_126502.1:n.884A>C
XM_005260617.2:c.803A>C	XP_005260674.1:p.Glu268Ala
XM_005260619.2:c.647A>C	XP_005260676.1:p.Glu216Ala
XR_936660.1:n.791A>C
NM_001322421.1:c.803A>C	NP_001309350.1:p.Glu268Ala
NM_001322422.1:c.635A>C	NP_001309351.1:p.Glu212Ala
NM_001362758.1:c.*117A>C	NP_001349687.1:n.*117A>C
NR_136327.1:n.787A>C
XM_005260619.3:c.647A>C	XP_005260676.1:p.Glu216Ala
XM_017028135.1:c.826A>C	XP_016883624.1:p.Arg276=
XM_017028136.1:c.724A>C	XP_016883625.1:p.Arg242=
NM_001250.6:c.791A>C MANE Select	NP_001241.1:p.Glu264Ala
NM_001302753.2:c.*117A>C	NP_001289682.1:n.*117A>C
NM_001322421.2:c.803A>C	NP_001309350.1:p.Glu268Ala
NM_001322422.2:c.635A>C	NP_001309351.1:p.Glu212Ala
NM_001362758.2:c.*117A>C	NP_001349687.1:n.*117A>C
NM_152854.4:c.*117A>C	NP_690593.1:n.*117A>C
NR_126502.2:n.824A>C
NR_136327.2:n.727A>C