Canonical Allele Identifier: CA2460412379
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659355T= , CM000685.2:g.136659355T= GRCh38
NC_000023.10:g.135741514T= , CM000685.1:g.135741514T= GRCh37
NC_000023.9:g.135569180T= NCBI36
NG_007280.1:g.16179T= , LRG_141:g.16179T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*344T= ENSP00000512122.1:n.*344T=
ENST00000695725.1:c.*281T= ENSP00000512123.1:n.*281T=
ENST00000695726.1:n.2694T=
ENST00000695729.1:n.3529T=
ENST00000370629.7:c.726T= MANE Select ENSP00000359663.2:p.Thr242=
ENST00000370628.2:c.663T= ENSP00000359662.2:p.Thr221=
ENST00000370629.6:c.726T= ENSP00000359663.2:p.Thr242=
NM_000074.2:c.726T= , LRG_141t1:c.726T= NP_000065.1:p.Thr242=
NM_000074.3:c.726T= MANE Select NP_000065.1:p.Thr242=