Canonical Allele Identifier: CA2579712099
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659440_136659442del , CM000685.2:g.136659440_136659442del GRCh38
NC_000023.10:g.135741599_135741601del , CM000685.1:g.135741599_135741601del GRCh37
NC_000023.9:g.135569265_135569267del NCBI36
NG_007280.1:g.16264_16266del , LRG_141:g.16264_16266del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*429_*431del ENSP00000512122.1:n.*429_*431del
ENST00000695725.1:c.*366_*368del ENSP00000512123.1:n.*366_*368del
ENST00000695726.1:n.2779_2781del
ENST00000695729.1:n.3614_3616del
ENST00000370629.7:c.*25_*27del MANE Select ENSP00000359663.2:n.*25_*27del
ENST00000370628.2:c.*25_*27del ENSP00000359662.2:n.*25_*27del
ENST00000370629.6:c.*25_*27del ENSP00000359663.2:n.*25_*27del
NM_000074.2:c.*25_*27del , LRG_141t1:c.*25_*27del NP_000065.1:n.*25_*27del
NM_000074.3:c.*25_*27del MANE Select NP_000065.1:n.*25_*27del