Canonical Allele Identifier: CA2695236795
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659284_136659286del , CM000685.2:g.136659284_136659286del GRCh38
NC_000023.10:g.135741443_135741445del , CM000685.1:g.135741443_135741445del GRCh37
NC_000023.9:g.135569109_135569111del NCBI36
NG_007280.1:g.16108_16110del , LRG_141:g.16108_16110del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*273_*275del ENSP00000512122.1:n.*273_*275del
ENST00000695725.1:c.*210_*212del ENSP00000512123.1:n.*210_*212del
ENST00000695726.1:n.2623_2625del
ENST00000695729.1:n.3458_3460del
ENST00000370629.7:c.655_657del MANE Select ENSP00000359663.2:p.Gly219del
ENST00000370628.2:c.592_594del ENSP00000359662.2:p.Gly198del
ENST00000370629.6:c.655_657del ENSP00000359663.2:p.Gly219del
NM_000074.2:c.655_657del , LRG_141t1:c.655_657del NP_000065.1:p.Gly219del
NM_000074.3:c.655_657del MANE Select NP_000065.1:p.Gly219del