Canonical Allele Identifier: CA2695236788
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659228del , CM000685.2:g.136659228del GRCh38
NC_000023.10:g.135741387del , CM000685.1:g.135741387del GRCh37
NC_000023.9:g.135569053del NCBI36
NG_007280.1:g.16052del , LRG_141:g.16052del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*217del ENSP00000512122.1:n.*217del
ENST00000695725.1:c.*154del ENSP00000512123.1:n.*154del
ENST00000695726.1:n.2567del
ENST00000695729.1:n.3402del
ENST00000370629.7:c.599del MANE Select ENSP00000359663.2:p.Arg200AsnfsTer?
ENST00000370628.2:c.536del ENSP00000359662.2:p.Arg179AsnfsTer?
ENST00000370629.6:c.599del ENSP00000359663.2:p.Arg200AsnfsTer?
NM_000074.2:c.599del , LRG_141t1:c.599del NP_000065.1:p.Arg200AsnfsTer?
NM_000074.3:c.599del MANE Select NP_000065.1:p.Arg200AsnfsTer?