Canonical Allele Identifier: CA2695236779
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659168del , CM000685.2:g.136659168del GRCh38
NC_000023.10:g.135741327del , CM000685.1:g.135741327del GRCh37
NC_000023.9:g.135568993del NCBI36
NG_007280.1:g.15992del , LRG_141:g.15992del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*157del ENSP00000512122.1:n.*157del
ENST00000695725.1:c.*94del ENSP00000512123.1:n.*94del
ENST00000695726.1:n.2507del
ENST00000695729.1:n.3342del
ENST00000370629.7:c.539del MANE Select ENSP00000359663.2:p.Asn180IlefsTer11
ENST00000370628.2:c.476del ENSP00000359662.2:p.Asn159IlefsTer11
ENST00000370629.6:c.539del ENSP00000359663.2:p.Asn180IlefsTer11
NM_000074.2:c.539del , LRG_141t1:c.539del NP_000065.1:p.Asn180IlefsTer11
NM_000074.3:c.539del MANE Select NP_000065.1:p.Asn180IlefsTer11