Canonical Allele Identifier: CA9888547
Gene: CD40 HGNC NCBI

Linked Data

dbSNP Id: rs778043845

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46128270C>T , CM000682.2:g.46128270C>T GRCh38
NC_000020.10:g.44756909C>T , CM000682.1:g.44756909C>T GRCh37
NC_000020.9:g.44190316C>T NCBI36
NG_007279.1:g.15004C>T , LRG_40:g.15004C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.648+46C>T ENSP00000512095.1:n.648+46C>T
ENST00000489304.6:c.729+46C>T ENSP00000512096.1:n.729+46C>T
ENST00000695670.1:n.627+34C>T
ENST00000695671.1:c.686+46C>T ENSP00000512093.1:n.686+46C>T
ENST00000695674.1:n.1125+46C>T
ENST00000695675.1:n.2522+46C>T
ENST00000372285.8:c.646+46C>T MANE Select ENSP00000361359.3:n.646+46C>T
ENST00000372276.7:c.584+46C>T ENSP00000361350.3:n.584+46C>T
ENST00000372285.7:c.646+46C>T ENSP00000361359.3:n.646+46C>T
ENST00000466205.5:c.548+46C>T
ENST00000477696.5:n.619+46C>T
ENST00000489304.5:n.722+46C>T
ENST00000620709.4:c.*193+46C>T ENSP00000484074.1:n.*193+46C>T
NM_001250.5:c.646+46C>T NP_001241.1:n.646+46C>T
NM_001302753.1:c.686+46C>T NP_001289682.1:n.686+46C>T
NM_152854.3:c.584+46C>T NP_690593.1:n.584+46C>T
NR_126502.1:n.739+46C>T
XM_005260617.2:c.658+34C>T XP_005260674.1:n.658+34C>T
XM_005260619.2:c.502+34C>T XP_005260676.1:n.502+34C>T
XR_936660.1:n.646+46C>T
NM_001322421.1:c.658+34C>T NP_001309350.1:n.658+34C>T
NM_001322422.1:c.490+46C>T NP_001309351.1:n.490+46C>T
NM_001362758.1:c.646+46C>T NP_001349687.1:n.646+46C>T
NR_136327.1:n.642+46C>T
XM_005260619.3:c.502+34C>T XP_005260676.1:n.502+34C>T
XM_017028135.1:c.686+46C>T XP_016883624.1:n.686+46C>T
XM_017028136.1:c.584+46C>T XP_016883625.1:n.584+46C>T
NM_001250.6:c.646+46C>T MANE Select NP_001241.1:n.646+46C>T
NM_001302753.2:c.686+46C>T NP_001289682.1:n.686+46C>T
NM_001322421.2:c.658+34C>T NP_001309350.1:n.658+34C>T
NM_001322422.2:c.490+46C>T NP_001309351.1:n.490+46C>T
NM_001362758.2:c.646+46C>T NP_001349687.1:n.646+46C>T
NM_152854.4:c.584+46C>T NP_690593.1:n.584+46C>T
NR_126502.2:n.679+46C>T
NR_136327.2:n.582+46C>T