Canonical Allele Identifier: CA414756358
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659288A>G , CM000685.2:g.136659288A>G GRCh38
NC_000023.10:g.135741447A>G , CM000685.1:g.135741447A>G GRCh37
NC_000023.9:g.135569113A>G NCBI36
NG_007280.1:g.16112A>G , LRG_141:g.16112A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*277A>G ENSP00000512122.1:n.*277A>G
ENST00000695725.1:c.*214A>G ENSP00000512123.1:n.*214A>G
ENST00000695726.1:n.2627A>G
ENST00000695729.1:n.3462A>G
ENST00000370629.7:c.659A>G MANE Select ENSP00000359663.2:p.Gln220Arg
ENST00000370628.2:c.596A>G ENSP00000359662.2:p.Gln199Arg
ENST00000370629.6:c.659A>G ENSP00000359663.2:p.Gln220Arg
NM_000074.2:c.659A>G , LRG_141t1:c.659A>G NP_000065.1:p.Gln220Arg
NM_000074.3:c.659A>G MANE Select NP_000065.1:p.Gln220Arg