Canonical Allele Identifier: CA409212399

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44757665C>G (hg19) ; chr20:g.46129026C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46129026C>G , CM000682.2:g.46129026C>G	GRCh38
NC_000020.10:g.44757665C>G , CM000682.1:g.44757665C>G	GRCh37
NC_000020.9:g.44191072C>G	NCBI36
NG_007279.1:g.15760C>G , LRG_40:g.15760C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000489304.6:c.903C>G	ENSP00000512096.1:n.903C>G
ENST00000695675.1:n.2696C>G
ENST00000372285.8:c.820C>G MANE Select	ENSP00000361359.3:p.Gln274Glu
ENST00000372276.7:c.*146C>G	ENSP00000361350.3:n.*146C>G
ENST00000372285.7:c.820C>G	ENSP00000361359.3:p.Gln274Glu
ENST00000466205.5:c.722C>G
ENST00000489304.5:n.896C>G
ENST00000620709.4:c.*367C>G	ENSP00000484074.1:n.*367C>G
NM_001250.5:c.820C>G	NP_001241.1:p.Gln274Glu
NM_001302753.1:c.*146C>G	NP_001289682.1:n.*146C>G
NM_152854.3:c.*146C>G	NP_690593.1:n.*146C>G
NR_126502.1:n.913C>G
XM_005260617.2:c.832C>G	XP_005260674.1:p.Gln278Glu
XM_005260619.2:c.676C>G	XP_005260676.1:p.Gln226Glu
XR_936660.1:n.820C>G
NM_001322421.1:c.832C>G	NP_001309350.1:p.Gln278Glu
NM_001322422.1:c.664C>G	NP_001309351.1:p.Gln222Glu
NM_001362758.1:c.*146C>G	NP_001349687.1:n.*146C>G
NR_136327.1:n.816C>G
XM_005260619.3:c.676C>G	XP_005260676.1:p.Gln226Glu
XM_017028135.1:c.855C>G	XP_016883624.1:p.Cys285Trp
XM_017028136.1:c.753C>G	XP_016883625.1:p.Cys251Trp
NM_001250.6:c.820C>G MANE Select	NP_001241.1:p.Gln274Glu
NM_001302753.2:c.*146C>G	NP_001289682.1:n.*146C>G
NM_001322421.2:c.832C>G	NP_001309350.1:p.Gln278Glu
NM_001322422.2:c.664C>G	NP_001309351.1:p.Gln222Glu
NM_001362758.2:c.*146C>G	NP_001349687.1:n.*146C>G
NM_152854.4:c.*146C>G	NP_690593.1:n.*146C>G
NR_126502.2:n.853C>G
NR_136327.2:n.756C>G