Canonical Allele Identifier: CA2695236761
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659065_136659067del , CM000685.2:g.136659065_136659067del GRCh38
NC_000023.10:g.135741224_135741226del , CM000685.1:g.135741224_135741226del GRCh37
NC_000023.9:g.135568890_135568892del NCBI36
NG_007280.1:g.15889_15891del , LRG_141:g.15889_15891del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*54_*56del ENSP00000512122.1:n.*54_*56del
ENST00000695725.1:c.183_185del ENSP00000512123.1:p.Thr62del
ENST00000695726.1:n.2404_2406del
ENST00000695729.1:n.3239_3241del
ENST00000370629.7:c.436_438del MANE Select ENSP00000359663.2:p.Tyr146del
ENST00000370628.2:c.373_375del ENSP00000359662.2:p.Tyr125del
ENST00000370629.6:c.436_438del ENSP00000359663.2:p.Tyr146del
NM_000074.2:c.436_438del , LRG_141t1:c.436_438del NP_000065.1:p.Tyr146del
NM_000074.3:c.436_438del MANE Select NP_000065.1:p.Tyr146del