Canonical Allele Identifier: CA414756394
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659294C>G , CM000685.2:g.136659294C>G GRCh38
NC_000023.10:g.135741453C>G , CM000685.1:g.135741453C>G GRCh37
NC_000023.9:g.135569119C>G NCBI36
NG_007280.1:g.16118C>G , LRG_141:g.16118C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*283C>G ENSP00000512122.1:n.*283C>G
ENST00000695725.1:c.*220C>G ENSP00000512123.1:n.*220C>G
ENST00000695726.1:n.2633C>G
ENST00000695729.1:n.3468C>G
ENST00000370629.7:c.665C>G MANE Select ENSP00000359663.2:p.Ser222Cys
ENST00000370628.2:c.602C>G ENSP00000359662.2:p.Ser201Cys
ENST00000370629.6:c.665C>G ENSP00000359663.2:p.Ser222Cys
NM_000074.2:c.665C>G , LRG_141t1:c.665C>G NP_000065.1:p.Ser222Cys
NM_000074.3:c.665C>G MANE Select NP_000065.1:p.Ser222Cys