Canonical Allele Identifier: CA2695236770
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659137_136659145del , CM000685.2:g.136659137_136659145del GRCh38
NC_000023.10:g.135741296_135741304del , CM000685.1:g.135741296_135741304del GRCh37
NC_000023.9:g.135568962_135568970del NCBI36
NG_007280.1:g.15961_15969del , LRG_141:g.15961_15969del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*126_*134del ENSP00000512122.1:n.*126_*134del
ENST00000695725.1:c.*63_*71del ENSP00000512123.1:n.*63_*71del
ENST00000695726.1:n.2476_2484del
ENST00000695729.1:n.3311_3319del
ENST00000370629.7:c.508_516del MANE Select ENSP00000359663.2:p.Tyr170_Tyr172del
ENST00000370628.2:c.445_453del ENSP00000359662.2:p.Tyr149_Tyr151del
ENST00000370629.6:c.508_516del ENSP00000359663.2:p.Tyr170_Tyr172del
NM_000074.2:c.508_516del , LRG_141t1:c.508_516del NP_000065.1:p.Tyr170_Tyr172del
NM_000074.3:c.508_516del MANE Select NP_000065.1:p.Tyr170_Tyr172del