Canonical Allele Identifier: CA414755809
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659155A>T , CM000685.2:g.136659155A>T GRCh38
NC_000023.10:g.135741314A>T , CM000685.1:g.135741314A>T GRCh37
NC_000023.9:g.135568980A>T NCBI36
NG_007280.1:g.15979A>T , LRG_141:g.15979A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*144A>T ENSP00000512122.1:n.*144A>T
ENST00000695725.1:c.*81A>T ENSP00000512123.1:n.*81A>T
ENST00000695726.1:n.2494A>T
ENST00000695729.1:n.3329A>T
ENST00000370629.7:c.526A>T MANE Select ENSP00000359663.2:p.Thr176Ser
ENST00000370628.2:c.463A>T ENSP00000359662.2:p.Thr155Ser
ENST00000370629.6:c.526A>T ENSP00000359663.2:p.Thr176Ser
NM_000074.2:c.526A>T , LRG_141t1:c.526A>T NP_000065.1:p.Thr176Ser
NM_000074.3:c.526A>T MANE Select NP_000065.1:p.Thr176Ser