Canonical Allele Identifier: CA2695236772
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659140_136659153del , CM000685.2:g.136659140_136659153del GRCh38
NC_000023.10:g.135741299_135741312del , CM000685.1:g.135741299_135741312del GRCh37
NC_000023.9:g.135568965_135568978del NCBI36
NG_007280.1:g.15964_15977del , LRG_141:g.15964_15977del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*129_*142del ENSP00000512122.1:n.*129_*142del
ENST00000695725.1:c.*66_*79del ENSP00000512123.1:n.*66_*79del
ENST00000695726.1:n.2479_2492del
ENST00000695729.1:n.3314_3327del
ENST00000370629.7:c.511_524del MANE Select ENSP00000359663.2:p.Ile171HisfsTer25
ENST00000370628.2:c.448_461del ENSP00000359662.2:p.Ile150HisfsTer25
ENST00000370629.6:c.511_524del ENSP00000359663.2:p.Ile171HisfsTer25
NM_000074.2:c.511_524del , LRG_141t1:c.511_524del NP_000065.1:p.Ile171HisfsTer25
NM_000074.3:c.511_524del MANE Select NP_000065.1:p.Ile171HisfsTer25