Canonical Allele Identifier: CA10528072
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs771141566

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648400A>G , CM000685.2:g.136648400A>G GRCh38
NC_000023.10:g.135730559A>G , CM000685.1:g.135730559A>G GRCh37
NC_000023.9:g.135558225A>G NCBI36
NG_007280.1:g.5224A>G , LRG_141:g.5224A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.152A>G ENSP00000512122.1:p.Asp51Gly
ENST00000695725.1:c.152A>G ENSP00000512123.1:p.Asp51Gly
ENST00000695726.1:n.195A>G
ENST00000695727.1:n.139A>G
ENST00000695728.1:n.139A>G
ENST00000370629.7:c.152A>G MANE Select ENSP00000359663.2:p.Asp51Gly
ENST00000370628.2:c.152A>G ENSP00000359662.2:p.Asp51Gly
ENST00000370629.6:c.152A>G ENSP00000359663.2:p.Asp51Gly
NM_000074.2:c.152A>G , LRG_141t1:c.152A>G NP_000065.1:p.Asp51Gly
NM_000074.3:c.152A>G MANE Select NP_000065.1:p.Asp51Gly