Canonical Allele Identifier: CA409212499

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757677T>C (hg19) ; chr20:g.46129038T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129038T>C , CM000682.2:g.46129038T>C	GRCh38
NC_000020.10:g.44757677T>C , CM000682.1:g.44757677T>C	GRCh37
NC_000020.9:g.44191084T>C	NCBI36
NG_007279.1:g.15772T>C , LRG_40:g.15772T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.915T>C	ENSP00000512096.1:n.915T>C
ENST00000695675.1:n.2708T>C
ENST00000372285.8:c.832T>C MANE Select	ENSP00000361359.3:p.Ter278Arg
ENST00000372276.7:c.*158T>C	ENSP00000361350.3:n.*158T>C
ENST00000372285.7:c.832T>C	ENSP00000361359.3:p.Ter278Arg
ENST00000466205.5:c.734T>C
ENST00000489304.5:n.908T>C
ENST00000620709.4:c.*379T>C	ENSP00000484074.1:n.*379T>C
NM_001250.5:c.832T>C	NP_001241.1:p.Ter278Arg
NM_001302753.1:c.*158T>C	NP_001289682.1:n.*158T>C
NM_152854.3:c.*158T>C	NP_690593.1:n.*158T>C
NR_126502.1:n.925T>C
XM_005260617.2:c.844T>C	XP_005260674.1:p.Ter282Arg
XM_005260619.2:c.688T>C	XP_005260676.1:p.Ter230Arg
XR_936660.1:n.832T>C
NM_001322421.1:c.844T>C	NP_001309350.1:p.Ter282Arg
NM_001322422.1:c.676T>C	NP_001309351.1:p.Ter226Arg
NM_001362758.1:c.*158T>C	NP_001349687.1:n.*158T>C
NR_136327.1:n.828T>C
XM_005260619.3:c.688T>C	XP_005260676.1:p.Ter230Arg
XM_017028135.1:c.867T>C	XP_016883624.1:p.Ser289=
XM_017028136.1:c.765T>C	XP_016883625.1:p.Ser255=
NM_001250.6:c.832T>C MANE Select	NP_001241.1:p.Ter278Arg
NM_001302753.2:c.*158T>C	NP_001289682.1:n.*158T>C
NM_001322421.2:c.844T>C	NP_001309350.1:p.Ter282Arg
NM_001322422.2:c.676T>C	NP_001309351.1:p.Ter226Arg
NM_001362758.2:c.*158T>C	NP_001349687.1:n.*158T>C
NM_152854.4:c.*158T>C	NP_690593.1:n.*158T>C
NR_126502.2:n.865T>C
NR_136327.2:n.768T>C