Canonical Allele Identifier: CA409205330
Gene: CD40 HGNC NCBI

Linked Data

dbSNP Id: rs1464002562

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46122700G>T , CM000682.2:g.46122700G>T GRCh38
NC_000020.10:g.44751339G>T , CM000682.1:g.44751339G>T GRCh37
NC_000020.9:g.44184746G>T NCBI36
NG_007279.1:g.9434G>T , LRG_40:g.9434G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.443G>T ENSP00000512095.1:n.443G>T
ENST00000489304.6:c.347G>T ENSP00000512096.1:p.Cys116Phe
ENST00000695669.1:n.420G>T
ENST00000695670.1:n.327G>T
ENST00000695671.1:c.347G>T ENSP00000512093.1:p.Cys116Phe
ENST00000695672.1:n.272G>T
ENST00000695673.1:n.212G>T
ENST00000372285.8:c.347G>T MANE Select ENSP00000361359.3:p.Cys116Phe
ENST00000372276.7:c.347G>T ENSP00000361350.3:p.Cys116Phe
ENST00000372285.7:c.347G>T ENSP00000361359.3:p.Cys116Phe
ENST00000461171.1:n.132G>T
ENST00000466205.5:c.343G>T
ENST00000477696.5:n.414G>T
ENST00000489304.5:n.340G>T
ENST00000620709.4:c.347G>T ENSP00000484074.1:p.Cys116Phe
NM_001250.5:c.347G>T NP_001241.1:p.Cys116Phe
NM_001302753.1:c.347G>T NP_001289682.1:p.Cys116Phe
NM_152854.3:c.347G>T NP_690593.1:p.Cys116Phe
NR_126502.1:n.437G>T
XM_005260617.2:c.347G>T XP_005260674.1:p.Cys116Phe
XM_005260619.2:c.347G>T XP_005260676.1:p.Cys116Phe
XM_011529109.1:c.347G>T XP_011527411.1:p.Cys116Phe
XR_936660.1:n.441G>T
NM_001322421.1:c.347G>T NP_001309350.1:p.Cys116Phe
NM_001322422.1:c.347G>T NP_001309351.1:p.Cys116Phe
NM_001362758.1:c.347G>T NP_001349687.1:p.Cys116Phe
NR_136327.1:n.437G>T
XM_005260619.3:c.347G>T XP_005260676.1:p.Cys116Phe
XM_011529109.2:c.347G>T XP_011527411.1:p.Cys116Phe
XM_017028135.1:c.347G>T XP_016883624.1:p.Cys116Phe
XM_017028136.1:c.347G>T XP_016883625.1:p.Cys116Phe
NM_001250.6:c.347G>T MANE Select NP_001241.1:p.Cys116Phe
NM_001302753.2:c.347G>T NP_001289682.1:p.Cys116Phe
NM_001322421.2:c.347G>T NP_001309350.1:p.Cys116Phe
NM_001322422.2:c.347G>T NP_001309351.1:p.Cys116Phe
NM_001362758.2:c.347G>T NP_001349687.1:p.Cys116Phe
NM_152854.4:c.347G>T NP_690593.1:p.Cys116Phe
NR_126502.2:n.377G>T
NR_136327.2:n.377G>T