Canonical Allele Identifier: CA510657887

Gene: CD40

Linked Data

• gnomAD v4: 20-46129034-A-G
• MyVariant Identifiers: chr20:g.44757673A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129034A>G , CM000682.2:g.46129034A>G	GRCh38
NC_000020.10:g.44757673A>G , CM000682.1:g.44757673A>G	GRCh37
NC_000020.9:g.44191080A>G	NCBI36
NG_007279.1:g.15768A>G , LRG_40:g.15768A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.911A>G	ENSP00000512096.1:n.911A>G
ENST00000695675.1:n.2704A>G
ENST00000372285.8:c.828A>G MANE Select	ENSP00000361359.3:p.Arg276=
ENST00000372276.7:c.*154A>G	ENSP00000361350.3:n.*154A>G
ENST00000372285.7:c.828A>G	ENSP00000361359.3:p.Arg276=
ENST00000466205.5:c.730A>G
ENST00000489304.5:n.904A>G
ENST00000620709.4:c.*375A>G	ENSP00000484074.1:n.*375A>G
NM_001250.5:c.828A>G	NP_001241.1:p.Arg276=
NM_001302753.1:c.*154A>G	NP_001289682.1:n.*154A>G
NM_152854.3:c.*154A>G	NP_690593.1:n.*154A>G
NR_126502.1:n.921A>G
XM_005260617.2:c.840A>G	XP_005260674.1:p.Arg280=
XM_005260619.2:c.684A>G	XP_005260676.1:p.Arg228=
XR_936660.1:n.828A>G
NM_001322421.1:c.840A>G	NP_001309350.1:p.Arg280=
NM_001322422.1:c.672A>G	NP_001309351.1:p.Arg224=
NM_001362758.1:c.*154A>G	NP_001349687.1:n.*154A>G
NR_136327.1:n.824A>G
XM_005260619.3:c.684A>G	XP_005260676.1:p.Arg228=
XM_017028135.1:c.863A>G	XP_016883624.1:p.Asp288Gly
XM_017028136.1:c.761A>G	XP_016883625.1:p.Asp254Gly
NM_001250.6:c.828A>G MANE Select	NP_001241.1:p.Arg276=
NM_001302753.2:c.*154A>G	NP_001289682.1:n.*154A>G
NM_001322421.2:c.840A>G	NP_001309350.1:p.Arg280=
NM_001322422.2:c.672A>G	NP_001309351.1:p.Arg224=
NM_001362758.2:c.*154A>G	NP_001349687.1:n.*154A>G
NM_152854.4:c.*154A>G	NP_690593.1:n.*154A>G
NR_126502.2:n.861A>G
NR_136327.2:n.764A>G