Canonical Allele Identifier: CA2695236790
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659245_136659248del , CM000685.2:g.136659245_136659248del GRCh38
NC_000023.10:g.135741404_135741407del , CM000685.1:g.135741404_135741407del GRCh37
NC_000023.9:g.135569070_135569073del NCBI36
NG_007280.1:g.16069_16072del , LRG_141:g.16069_16072del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*234_*237del ENSP00000512122.1:n.*234_*237del
ENST00000695725.1:c.*171_*174del ENSP00000512123.1:n.*171_*174del
ENST00000695726.1:n.2584_2587del
ENST00000695729.1:n.3419_3422del
ENST00000370629.7:c.616_619del MANE Select ENSP00000359663.2:p.Leu206GlufsTer?
ENST00000370628.2:c.553_556del ENSP00000359662.2:p.Leu185GlufsTer?
ENST00000370629.6:c.616_619del ENSP00000359663.2:p.Leu206GlufsTer?
NM_000074.2:c.616_619del , LRG_141t1:c.616_619del NP_000065.1:p.Leu206GlufsTer?
NM_000074.3:c.616_619del MANE Select NP_000065.1:p.Leu206GlufsTer?