Canonical Allele Identifier: CA2695236797
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659309_136659311del , CM000685.2:g.136659309_136659311del GRCh38
NC_000023.10:g.135741468_135741470del , CM000685.1:g.135741468_135741470del GRCh37
NC_000023.9:g.135569134_135569136del NCBI36
NG_007280.1:g.16133_16135del , LRG_141:g.16133_16135del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*298_*300del ENSP00000512122.1:n.*298_*300del
ENST00000695725.1:c.*235_*237del ENSP00000512123.1:n.*235_*237del
ENST00000695726.1:n.2648_2650del
ENST00000695729.1:n.3483_3485del
ENST00000370629.7:c.680_682del MANE Select ENSP00000359663.2:p.Gly227del
ENST00000370628.2:c.617_619del ENSP00000359662.2:p.Gly206del
ENST00000370629.6:c.680_682del ENSP00000359663.2:p.Gly227del
NM_000074.2:c.680_682del , LRG_141t1:c.680_682del NP_000065.1:p.Gly227del
NM_000074.3:c.680_682del MANE Select NP_000065.1:p.Gly227del