Canonical Allele Identifier: CA2695236766
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659124_136659128del , CM000685.2:g.136659124_136659128del GRCh38
NC_000023.10:g.135741283_135741287del , CM000685.1:g.135741283_135741287del GRCh37
NC_000023.9:g.135568949_135568953del NCBI36
NG_007280.1:g.15948_15952del , LRG_141:g.15948_15952del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*113_*117del ENSP00000512122.1:n.*113_*117del
ENST00000695725.1:c.*50_*54del ENSP00000512123.1:n.*50_*54del
ENST00000695726.1:n.2463_2467del
ENST00000695729.1:n.3298_3302del
ENST00000370629.7:c.495_499del MANE Select ENSP00000359663.2:p.Gln166ThrfsTer?
ENST00000370628.2:c.432_436del ENSP00000359662.2:p.Gln145ThrfsTer?
ENST00000370629.6:c.495_499del ENSP00000359663.2:p.Gln166ThrfsTer?
NM_000074.2:c.495_499del , LRG_141t1:c.495_499del NP_000065.1:p.Gln166ThrfsTer?
NM_000074.3:c.495_499del MANE Select NP_000065.1:p.Gln166ThrfsTer?