Canonical Allele Identifier: CA636177229

Gene: CD40

Linked Data

• dbSNP Id: rs1261623149
• gnomAD v2: 20-44757771-G-C
• gnomAD v4: 20-46129132-G-C
• MyVariant Identifiers: chr20:g.44757771G>C (hg19) ; chr20:g.46129132G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129132G>C , CM000682.2:g.46129132G>C	GRCh38
NC_000020.10:g.44757771G>C , CM000682.1:g.44757771G>C	GRCh37
NC_000020.9:g.44191178G>C	NCBI36
NG_007279.1:g.15866G>C , LRG_40:g.15866G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.1009G>C	ENSP00000512096.1:n.1009G>C
ENST00000695675.1:n.2802G>C
ENST00000372285.8:c.*92G>C MANE Select	ENSP00000361359.3:n.*92G>C
ENST00000372276.7:c.*252G>C	ENSP00000361350.3:n.*252G>C
ENST00000372285.7:c.*92G>C	ENSP00000361359.3:n.*92G>C
ENST00000489304.5:n.1002G>C
ENST00000620709.4:c.*473G>C	ENSP00000484074.1:n.*473G>C
NM_001250.5:c.*92G>C	NP_001241.1:n.*92G>C
NM_001302753.1:c.*252G>C	NP_001289682.1:n.*252G>C
NM_152854.3:c.*252G>C	NP_690593.1:n.*252G>C
NR_126502.1:n.1019G>C
XM_005260617.2:c.*92G>C	XP_005260674.1:n.*92G>C
XM_005260619.2:c.*92G>C	XP_005260676.1:n.*92G>C
NM_001322421.1:c.*92G>C	NP_001309350.1:n.*92G>C
NM_001322422.1:c.*92G>C	NP_001309351.1:n.*92G>C
NM_001362758.1:c.*252G>C	NP_001349687.1:n.*252G>C
NR_136327.1:n.922G>C
XM_005260619.3:c.*92G>C	XP_005260676.1:n.*92G>C
XM_017028135.1:c.961G>C	XP_016883624.1:p.Gly321Arg
XM_017028136.1:c.859G>C	XP_016883625.1:p.Gly287Arg
NM_001250.6:c.*92G>C MANE Select	NP_001241.1:n.*92G>C
NM_001302753.2:c.*252G>C	NP_001289682.1:n.*252G>C
NM_001322421.2:c.*92G>C	NP_001309350.1:n.*92G>C
NM_001322422.2:c.*92G>C	NP_001309351.1:n.*92G>C
NM_001362758.2:c.*252G>C	NP_001349687.1:n.*252G>C
NM_152854.4:c.*252G>C	NP_690593.1:n.*252G>C
NR_126502.2:n.959G>C
NR_136327.2:n.862G>C