Canonical Allele Identifier: CA414753576
Community Standard Title: NM_000074.3(CD40LG):c.268C>T (p.Gln90Ter)
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136650377C>T , CM000685.2:g.136650377C>T GRCh38
NC_000023.10:g.135732536C>T , CM000685.1:g.135732536C>T GRCh37
NC_000023.9:g.135560202C>T NCBI36
NG_007280.1:g.7201C>T , LRG_141:g.7201C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000074.3:c.268C>T MANE Select NP_000065.1:p.Gln90Ter
ENST00000370629.7:c.268C>T MANE Select ENSP00000359663.2:p.Gln90Ter
NM_000074.2:c.268C>T , LRG_141t1:c.268C>T NP_000065.1:p.Gln90Ter
ENST00000370628.2:c.268C>T ENSP00000359662.2:p.Gln90Ter
ENST00000370629.6:c.268C>T ENSP00000359663.2:p.Gln90Ter
ENST00000695724.1:c.268C>T ENSP00000512122.1:p.Gln90Ter
ENST00000695725.1:c.156+1973C>T ENSP00000512123.1:n.156+1973C>T
ENST00000695726.1:n.311C>T
ENST00000695727.1:n.255C>T
ENST00000695728.1:n.255C>T