Canonical Allele Identifier: CA315654906

Gene: CD40

Linked Data

• dbSNP Id: rs913525522
• gnomAD v4: 20-46129044-T-C
• MyVariant Identifiers: chr20:g.44757683T>C (hg19) ; chr20:g.46129044T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129044T>C , CM000682.2:g.46129044T>C	GRCh38
NC_000020.10:g.44757683T>C , CM000682.1:g.44757683T>C	GRCh37
NC_000020.9:g.44191090T>C	NCBI36
NG_007279.1:g.15778T>C , LRG_40:g.15778T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.921T>C	ENSP00000512096.1:n.921T>C
ENST00000695675.1:n.2714T>C
ENST00000372285.8:c.*4T>C MANE Select	ENSP00000361359.3:n.*4T>C
ENST00000372276.7:c.*164T>C	ENSP00000361350.3:n.*164T>C
ENST00000372285.7:c.*4T>C	ENSP00000361359.3:n.*4T>C
ENST00000466205.5:c.740T>C
ENST00000489304.5:n.914T>C
ENST00000620709.4:c.*385T>C	ENSP00000484074.1:n.*385T>C
NM_001250.5:c.*4T>C	NP_001241.1:n.*4T>C
NM_001302753.1:c.*164T>C	NP_001289682.1:n.*164T>C
NM_152854.3:c.*164T>C	NP_690593.1:n.*164T>C
NR_126502.1:n.931T>C
XM_005260617.2:c.*4T>C	XP_005260674.1:n.*4T>C
XM_005260619.2:c.*4T>C	XP_005260676.1:n.*4T>C
XR_936660.1:n.838T>C
NM_001322421.1:c.*4T>C	NP_001309350.1:n.*4T>C
NM_001322422.1:c.*4T>C	NP_001309351.1:n.*4T>C
NM_001362758.1:c.*164T>C	NP_001349687.1:n.*164T>C
NR_136327.1:n.834T>C
XM_005260619.3:c.*4T>C	XP_005260676.1:n.*4T>C
XM_017028135.1:c.873T>C	XP_016883624.1:p.Ala291=
XM_017028136.1:c.771T>C	XP_016883625.1:p.Ala257=
NM_001250.6:c.*4T>C MANE Select	NP_001241.1:n.*4T>C
NM_001302753.2:c.*164T>C	NP_001289682.1:n.*164T>C
NM_001322421.2:c.*4T>C	NP_001309350.1:n.*4T>C
NM_001322422.2:c.*4T>C	NP_001309351.1:n.*4T>C
NM_001362758.2:c.*164T>C	NP_001349687.1:n.*164T>C
NM_152854.4:c.*164T>C	NP_690593.1:n.*164T>C
NR_126502.2:n.871T>C
NR_136327.2:n.774T>C