Canonical Allele Identifier: CA414752798
Community Standard Title: NM_000074.3(CD40LG):c.166G>T (p.Glu56Ter)
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136650275G>T , CM000685.2:g.136650275G>T GRCh38
NC_000023.10:g.135732434G>T , CM000685.1:g.135732434G>T GRCh37
NC_000023.9:g.135560100G>T NCBI36
NG_007280.1:g.7099G>T , LRG_141:g.7099G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000074.3:c.166G>T MANE Select NP_000065.1:p.Glu56Ter
ENST00000370629.7:c.166G>T MANE Select ENSP00000359663.2:p.Glu56Ter
NM_000074.2:c.166G>T , LRG_141t1:c.166G>T NP_000065.1:p.Glu56Ter
ENST00000370628.2:c.166G>T ENSP00000359662.2:p.Glu56Ter
ENST00000370629.6:c.166G>T ENSP00000359663.2:p.Glu56Ter
ENST00000695724.1:c.166G>T ENSP00000512122.1:p.Glu56Ter
ENST00000695725.1:c.156+1871G>T ENSP00000512123.1:n.156+1871G>T
ENST00000695726.1:n.209G>T
ENST00000695727.1:n.153G>T
ENST00000695728.1:n.153G>T