Canonical Allele Identifier: CA657647732

Gene: CD40

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46128235A>G , CM000682.2:g.46128235A>G	GRCh38
NC_000020.10:g.44756874A>G , CM000682.1:g.44756874A>G	GRCh37
NC_000020.9:g.44190281A>G	NCBI36
NG_007279.1:g.14969A>G , LRG_40:g.14969A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477696.6:c.648+11A>G	ENSP00000512095.1:n.648+11A>G
ENST00000489304.6:c.729+11A>G	ENSP00000512096.1:n.729+11A>G
ENST00000695670.1:n.626A>G
ENST00000695671.1:c.686+11A>G	ENSP00000512093.1:n.686+11A>G
ENST00000695674.1:n.1125+11A>G
ENST00000695675.1:n.2522+11A>G
ENST00000372285.8:c.646+11A>G MANE Select	ENSP00000361359.3:n.646+11A>G
ENST00000372276.7:c.584+11A>G	ENSP00000361350.3:n.584+11A>G
ENST00000372285.7:c.646+11A>G	ENSP00000361359.3:n.646+11A>G
ENST00000466205.5:c.548+11A>G
ENST00000477696.5:n.619+11A>G
ENST00000489304.5:n.722+11A>G
ENST00000620709.4:c.*193+11A>G	ENSP00000484074.1:n.*193+11A>G
NM_001250.5:c.646+11A>G	NP_001241.1:n.646+11A>G
NM_001302753.1:c.686+11A>G	NP_001289682.1:n.686+11A>G
NM_152854.3:c.584+11A>G	NP_690593.1:n.584+11A>G
NR_126502.1:n.739+11A>G
XM_005260617.2:c.657A>G	XP_005260674.1:p.Ser219=
XM_005260619.2:c.501A>G	XP_005260676.1:p.Ser167=
XR_936660.1:n.646+11A>G
NM_001322421.1:c.657A>G	NP_001309350.1:p.Ser219=
NM_001322422.1:c.490+11A>G	NP_001309351.1:n.490+11A>G
NM_001362758.1:c.646+11A>G	NP_001349687.1:n.646+11A>G
NR_136327.1:n.642+11A>G
XM_005260619.3:c.501A>G	XP_005260676.1:p.Ser167=
XM_017028135.1:c.686+11A>G	XP_016883624.1:n.686+11A>G
XM_017028136.1:c.584+11A>G	XP_016883625.1:n.584+11A>G
NM_001250.6:c.646+11A>G MANE Select	NP_001241.1:n.646+11A>G
NM_001302753.2:c.686+11A>G	NP_001289682.1:n.686+11A>G
NM_001322421.2:c.657A>G	NP_001309350.1:p.Ser219=
NM_001322422.2:c.490+11A>G	NP_001309351.1:n.490+11A>G
NM_001362758.2:c.646+11A>G	NP_001349687.1:n.646+11A>G
NM_152854.4:c.584+11A>G	NP_690593.1:n.584+11A>G
NR_126502.2:n.679+11A>G
NR_136327.2:n.582+11A>G