Canonical Allele Identifier: CA2366533091
Gene: CD40 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46128202C= , CM000682.2:g.46128202C= GRCh38
NC_000020.10:g.44756841C= , CM000682.1:g.44756841C= GRCh37
NC_000020.9:g.44190248C= NCBI36
NG_007279.1:g.14936C= , LRG_40:g.14936C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000477696.6:c.626C= ENSP00000512095.1:n.626C=
ENST00000489304.6:c.707C= ENSP00000512096.1:n.707C=
ENST00000695670.1:n.593C=
ENST00000695671.1:c.664C= ENSP00000512093.1:p.Pro222=
ENST00000695674.1:n.1103C=
ENST00000695675.1:n.2500C=
ENST00000372285.8:c.624C= MANE Select ENSP00000361359.3:p.Ile208=
ENST00000372276.7:c.562C= ENSP00000361350.3:p.Pro188=
ENST00000372285.7:c.624C= ENSP00000361359.3:p.Ile208=
ENST00000466205.5:c.526C=
ENST00000477696.5:n.597C=
ENST00000489304.5:n.700C=
ENST00000620709.4:c.*171C= ENSP00000484074.1:n.*171C=
NM_001250.5:c.624C= NP_001241.1:p.Ile208=
NM_001302753.1:c.664C= NP_001289682.1:p.Pro222=
NM_152854.3:c.562C= NP_690593.1:p.Pro188=
NR_126502.1:n.717C=
XM_005260617.2:c.624C= XP_005260674.1:p.Ile208=
XM_005260619.2:c.468C= XP_005260676.1:p.Ile156=
XR_936660.1:n.624C=
NM_001322421.1:c.624C= NP_001309350.1:p.Ile208=
NM_001322422.1:c.468C= NP_001309351.1:p.Ile156=
NM_001362758.1:c.624C= NP_001349687.1:p.Ile208=
NR_136327.1:n.620C=
XM_005260619.3:c.468C= XP_005260676.1:p.Ile156=
XM_017028135.1:c.664C= XP_016883624.1:p.Pro222=
XM_017028136.1:c.562C= XP_016883625.1:p.Pro188=
NM_001250.6:c.624C= MANE Select NP_001241.1:p.Ile208=
NM_001302753.2:c.664C= NP_001289682.1:p.Pro222=
NM_001322421.2:c.624C= NP_001309350.1:p.Ile208=
NM_001322422.2:c.468C= NP_001309351.1:p.Ile156=
NM_001362758.2:c.624C= NP_001349687.1:p.Ile208=
NM_152854.4:c.562C= NP_690593.1:p.Pro188=
NR_126502.2:n.657C=
NR_136327.2:n.560C=