Canonical Allele Identifier: CA409200430

Gene: CD40

Linked Data

• MyVariant Identifiers: chr20:g.44746992C>G (hg19) ; chr20:g.46118353C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46118353C>G , CM000682.2:g.46118353C>G	GRCh38
NC_000020.10:g.44746992C>G , CM000682.1:g.44746992C>G	GRCh37
NC_000020.9:g.44180399C>G	NCBI36
NG_007279.1:g.5087C>G , LRG_40:g.5087C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000477696.6:c.10C>G	ENSP00000512095.1:p.Leu4Val
ENST00000489304.6:c.10C>G	ENSP00000512096.1:p.Leu4Val
ENST00000695669.1:n.83C>G
ENST00000695670.1:n.69C>G
ENST00000695671.1:c.10C>G	ENSP00000512093.1:p.Leu4Val
ENST00000695672.1:n.14C>G
ENST00000372285.8:c.10C>G MANE Select	ENSP00000361359.3:p.Leu4Val
ENST00000372276.7:c.10C>G	ENSP00000361350.3:p.Leu4Val
ENST00000372285.7:c.10C>G	ENSP00000361359.3:p.Leu4Val
ENST00000466205.5:c.6C>G
ENST00000489304.5:n.3C>G
ENST00000620709.4:c.10C>G	ENSP00000484074.1:p.Leu4Val
NM_001250.5:c.10C>G	NP_001241.1:p.Leu4Val
NM_001302753.1:c.10C>G	NP_001289682.1:p.Leu4Val
NM_152854.3:c.10C>G	NP_690593.1:p.Leu4Val
NR_126502.1:n.100C>G
XM_005260617.2:c.10C>G	XP_005260674.1:p.Leu4Val
XM_005260619.2:c.10C>G	XP_005260676.1:p.Leu4Val
XM_011529109.1:c.10C>G	XP_011527411.1:p.Leu4Val
XR_936660.1:n.104C>G
NM_001322421.1:c.10C>G	NP_001309350.1:p.Leu4Val
NM_001322422.1:c.10C>G	NP_001309351.1:p.Leu4Val
NM_001362758.1:c.10C>G	NP_001349687.1:p.Leu4Val
NR_136327.1:n.100C>G
XM_005260619.3:c.10C>G	XP_005260676.1:p.Leu4Val
XM_011529109.2:c.10C>G	XP_011527411.1:p.Leu4Val
XM_017028135.1:c.10C>G	XP_016883624.1:p.Leu4Val
XM_017028136.1:c.10C>G	XP_016883625.1:p.Leu4Val
NM_001250.6:c.10C>G MANE Select	NP_001241.1:p.Leu4Val
NM_001302753.2:c.10C>G	NP_001289682.1:p.Leu4Val
NM_001322421.2:c.10C>G	NP_001309350.1:p.Leu4Val
NM_001322422.2:c.10C>G	NP_001309351.1:p.Leu4Val
NM_001362758.2:c.10C>G	NP_001349687.1:p.Leu4Val
NM_152854.4:c.10C>G	NP_690593.1:p.Leu4Val
NR_126502.2:n.40C>G
NR_136327.2:n.40C>G