Canonical Allele Identifier: CA2695236803
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659388_136659396del , CM000685.2:g.136659388_136659396del GRCh38
NC_000023.10:g.135741547_135741555del , CM000685.1:g.135741547_135741555del GRCh37
NC_000023.9:g.135569213_135569221del NCBI36
NG_007280.1:g.16212_16220del , LRG_141:g.16212_16220del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*377_*385del ENSP00000512122.1:n.*377_*385del
ENST00000695725.1:c.*314_*322del ENSP00000512123.1:n.*314_*322del
ENST00000695726.1:n.2727_2735del
ENST00000695729.1:n.3562_3570del
ENST00000370629.7:c.759_767del MANE Select ENSP00000359663.2:p.Thr254_Phe256del
ENST00000370628.2:c.696_704del ENSP00000359662.2:p.Thr233_Phe235del
ENST00000370629.6:c.759_767del ENSP00000359663.2:p.Thr254_Phe256del
NM_000074.2:c.759_767del , LRG_141t1:c.759_767del NP_000065.1:p.Thr254_Phe256del
NM_000074.3:c.759_767del MANE Select NP_000065.1:p.Thr254_Phe256del