Canonical Allele Identifier: CA1139768465
Gene: CD40LG HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*157dup ENSP00000512122.1:n.*157dup
ENST00000695725.1:c.*94dup ENSP00000512123.1:n.*94dup
ENST00000695726.1:n.2507dup
ENST00000695729.1:n.3342dup
ENST00000370629.7:c.539dup MANE Select ENSP00000359663.2:p.Asn180LysfsTer21
ENST00000370628.2:c.476dup ENSP00000359662.2:p.Asn159LysfsTer21
ENST00000370629.6:c.539dup ENSP00000359663.2:p.Asn180LysfsTer21
NM_000074.2:c.539dup , LRG_141t1:c.539dup NP_000065.1:p.Asn180LysfsTer21
NM_000074.3:c.539dup MANE Select NP_000065.1:p.Asn180LysfsTer21