Canonical Allele Identifier: CA409212458

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757671A>T (hg19) ; chr20:g.46129032A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.909A>T	ENSP00000512096.1:n.909A>T
ENST00000695675.1:n.2702A>T
ENST00000372285.8:c.826A>T MANE Select	ENSP00000361359.3:p.Arg276Ter
ENST00000372276.7:c.*152A>T	ENSP00000361350.3:n.*152A>T
ENST00000372285.7:c.826A>T	ENSP00000361359.3:p.Arg276Ter
ENST00000466205.5:c.728A>T
ENST00000489304.5:n.902A>T
ENST00000620709.4:c.*373A>T	ENSP00000484074.1:n.*373A>T
NM_001250.5:c.826A>T	NP_001241.1:p.Arg276Ter
NM_001302753.1:c.*152A>T	NP_001289682.1:n.*152A>T
NM_152854.3:c.*152A>T	NP_690593.1:n.*152A>T
NR_126502.1:n.919A>T
XM_005260617.2:c.838A>T	XP_005260674.1:p.Arg280Ter
XM_005260619.2:c.682A>T	XP_005260676.1:p.Arg228Ter
XR_936660.1:n.826A>T
NM_001322421.1:c.838A>T	NP_001309350.1:p.Arg280Ter
NM_001322422.1:c.670A>T	NP_001309351.1:p.Arg224Ter
NM_001362758.1:c.*152A>T	NP_001349687.1:n.*152A>T
NR_136327.1:n.822A>T
XM_005260619.3:c.682A>T	XP_005260676.1:p.Arg228Ter
XM_017028135.1:c.861A>T	XP_016883624.1:p.Arg287Ser
XM_017028136.1:c.759A>T	XP_016883625.1:p.Arg253Ser
NM_001250.6:c.826A>T MANE Select	NP_001241.1:p.Arg276Ter
NM_001302753.2:c.*152A>T	NP_001289682.1:n.*152A>T
NM_001322421.2:c.838A>T	NP_001309350.1:p.Arg280Ter
NM_001322422.2:c.670A>T	NP_001309351.1:p.Arg224Ter
NM_001362758.2:c.*152A>T	NP_001349687.1:n.*152A>T
NM_152854.4:c.*152A>T	NP_690593.1:n.*152A>T
NR_126502.2:n.859A>T
NR_136327.2:n.762A>T