Canonical Allele Identifier: CA2580101588
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 2054209
ClinVar RCV Id: RCV002927819

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659385del , CM000685.2:g.136659385del GRCh38
NC_000023.10:g.135741544del , CM000685.1:g.135741544del GRCh37
NC_000023.9:g.135569210del NCBI36
NG_007280.1:g.16209del , LRG_141:g.16209del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*374del ENSP00000512122.1:n.*374del
ENST00000695725.1:c.*311del ENSP00000512123.1:n.*311del
ENST00000695726.1:n.2724del
ENST00000695729.1:n.3559del
ENST00000370629.7:c.756del MANE Select ENSP00000359663.2:p.Phe253SerfsTer?
ENST00000370628.2:c.693del ENSP00000359662.2:p.Phe232SerfsTer?
ENST00000370629.6:c.756del ENSP00000359663.2:p.Phe253SerfsTer?
NM_000074.2:c.756del , LRG_141t1:c.756del NP_000065.1:p.Phe253SerfsTer?
NM_000074.3:c.756del MANE Select NP_000065.1:p.Phe253SerfsTer?