Canonical Allele Identifier: CA2366529057
Gene: CD40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46118362C= , CM000682.2:g.46118362C= GRCh38
NC_000020.10:g.44747001C= , CM000682.1:g.44747001C= GRCh37
NC_000020.9:g.44180408C= NCBI36
NG_007279.1:g.5096C= , LRG_40:g.5096C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.19C= ENSP00000512095.1:p.Gln7=
ENST00000489304.6:c.19C= ENSP00000512096.1:p.Gln7=
ENST00000695669.1:n.92C=
ENST00000695670.1:n.78C=
ENST00000695671.1:c.19C= ENSP00000512093.1:p.Gln7=
ENST00000695672.1:n.23C=
ENST00000372285.8:c.19C= MANE Select ENSP00000361359.3:p.Gln7=
ENST00000372276.7:c.19C= ENSP00000361350.3:p.Gln7=
ENST00000372285.7:c.19C= ENSP00000361359.3:p.Gln7=
ENST00000466205.5:c.15C=
ENST00000489304.5:n.12C=
ENST00000620709.4:c.19C= ENSP00000484074.1:p.Gln7=
NM_001250.5:c.19C= NP_001241.1:p.Gln7=
NM_001302753.1:c.19C= NP_001289682.1:p.Gln7=
NM_152854.3:c.19C= NP_690593.1:p.Gln7=
NR_126502.1:n.109C=
XM_005260617.2:c.19C= XP_005260674.1:p.Gln7=
XM_005260619.2:c.19C= XP_005260676.1:p.Gln7=
XM_011529109.1:c.19C= XP_011527411.1:p.Gln7=
XR_936660.1:n.113C=
NM_001322421.1:c.19C= NP_001309350.1:p.Gln7=
NM_001322422.1:c.19C= NP_001309351.1:p.Gln7=
NM_001362758.1:c.19C= NP_001349687.1:p.Gln7=
NR_136327.1:n.109C=
XM_005260619.3:c.19C= XP_005260676.1:p.Gln7=
XM_011529109.2:c.19C= XP_011527411.1:p.Gln7=
XM_017028135.1:c.19C= XP_016883624.1:p.Gln7=
XM_017028136.1:c.19C= XP_016883625.1:p.Gln7=
NM_001250.6:c.19C= MANE Select NP_001241.1:p.Gln7=
NM_001302753.2:c.19C= NP_001289682.1:p.Gln7=
NM_001322421.2:c.19C= NP_001309350.1:p.Gln7=
NM_001322422.2:c.19C= NP_001309351.1:p.Gln7=
NM_001362758.2:c.19C= NP_001349687.1:p.Gln7=
NM_152854.4:c.19C= NP_690593.1:p.Gln7=
NR_126502.2:n.49C=
NR_136327.2:n.49C=