Canonical Allele Identifier: CA510657886

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757671A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129032A>C , CM000682.2:g.46129032A>C	GRCh38
NC_000020.10:g.44757671A>C , CM000682.1:g.44757671A>C	GRCh37
NC_000020.9:g.44191078A>C	NCBI36
NG_007279.1:g.15766A>C , LRG_40:g.15766A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.909A>C	ENSP00000512096.1:n.909A>C
ENST00000695675.1:n.2702A>C
ENST00000372285.8:c.826A>C MANE Select	ENSP00000361359.3:p.Arg276=
ENST00000372276.7:c.*152A>C	ENSP00000361350.3:n.*152A>C
ENST00000372285.7:c.826A>C	ENSP00000361359.3:p.Arg276=
ENST00000466205.5:c.728A>C
ENST00000489304.5:n.902A>C
ENST00000620709.4:c.*373A>C	ENSP00000484074.1:n.*373A>C
NM_001250.5:c.826A>C	NP_001241.1:p.Arg276=
NM_001302753.1:c.*152A>C	NP_001289682.1:n.*152A>C
NM_152854.3:c.*152A>C	NP_690593.1:n.*152A>C
NR_126502.1:n.919A>C
XM_005260617.2:c.838A>C	XP_005260674.1:p.Arg280=
XM_005260619.2:c.682A>C	XP_005260676.1:p.Arg228=
XR_936660.1:n.826A>C
NM_001322421.1:c.838A>C	NP_001309350.1:p.Arg280=
NM_001322422.1:c.670A>C	NP_001309351.1:p.Arg224=
NM_001362758.1:c.*152A>C	NP_001349687.1:n.*152A>C
NR_136327.1:n.822A>C
XM_005260619.3:c.682A>C	XP_005260676.1:p.Arg228=
XM_017028135.1:c.861A>C	XP_016883624.1:p.Arg287Ser
XM_017028136.1:c.759A>C	XP_016883625.1:p.Arg253Ser
NM_001250.6:c.826A>C MANE Select	NP_001241.1:p.Arg276=
NM_001302753.2:c.*152A>C	NP_001289682.1:n.*152A>C
NM_001322421.2:c.838A>C	NP_001309350.1:p.Arg280=
NM_001322422.2:c.670A>C	NP_001309351.1:p.Arg224=
NM_001362758.2:c.*152A>C	NP_001349687.1:n.*152A>C
NM_152854.4:c.*152A>C	NP_690593.1:n.*152A>C
NR_126502.2:n.859A>C
NR_136327.2:n.762A>C