Canonical Allele Identifier: CA2695236778
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659162del , CM000685.2:g.136659162del GRCh38
NC_000023.10:g.135741321del , CM000685.1:g.135741321del GRCh37
NC_000023.9:g.135568987del NCBI36
NG_007280.1:g.15986del , LRG_141:g.15986del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*151del ENSP00000512122.1:n.*151del
ENST00000695725.1:c.*88del ENSP00000512123.1:n.*88del
ENST00000695726.1:n.2501del
ENST00000695729.1:n.3336del
ENST00000370629.7:c.533del MANE Select ENSP00000359663.2:p.Cys178PhefsTer13
ENST00000370628.2:c.470del ENSP00000359662.2:p.Cys157PhefsTer13
ENST00000370629.6:c.533del ENSP00000359663.2:p.Cys178PhefsTer13
NM_000074.2:c.533del , LRG_141t1:c.533del NP_000065.1:p.Cys178PhefsTer13
NM_000074.3:c.533del MANE Select NP_000065.1:p.Cys178PhefsTer13