Canonical Allele Identifier: CA2823748780
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659305_136659306del , CM000685.2:g.136659305_136659306del GRCh38
NC_000023.10:g.135741464_135741465del , CM000685.1:g.135741464_135741465del GRCh37
NC_000023.9:g.135569130_135569131del NCBI36
NG_007280.1:g.16129_16130del , LRG_141:g.16129_16130del

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*294_*295del ENSP00000512122.1:n.*294_*295del
ENST00000695725.1:c.*231_*232del ENSP00000512123.1:n.*231_*232del
ENST00000695726.1:n.2644_2645del
ENST00000695729.1:n.3479_3480del
ENST00000370629.7:c.676_677del MANE Select ENSP00000359663.2:p.Gly226ArgfsTer4
ENST00000370628.2:c.613_614del ENSP00000359662.2:p.Gly205ArgfsTer4
ENST00000370629.6:c.676_677del ENSP00000359663.2:p.Gly226ArgfsTer4
NM_000074.2:c.676_677del , LRG_141t1:c.676_677del NP_000065.1:p.Gly226ArgfsTer4
NM_000074.3:c.676_677del MANE Select NP_000065.1:p.Gly226ArgfsTer4