Canonical Allele Identifier: CA414755594
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 633146
dbSNP Id: rs1569377744

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659058A>C , CM000685.2:g.136659058A>C GRCh38
NC_000023.10:g.135741217A>C , CM000685.1:g.135741217A>C GRCh37
NC_000023.9:g.135568883A>C NCBI36
NG_007280.1:g.15882A>C , LRG_141:g.15882A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*47A>C ENSP00000512122.1:n.*47A>C
ENST00000695725.1:c.176A>C ENSP00000512123.1:p.Lys59Thr
ENST00000695726.1:n.2397A>C
ENST00000695729.1:n.3232A>C
ENST00000370629.7:c.429A>C MANE Select ENSP00000359663.2:p.Lys143Asn
ENST00000370628.2:c.366A>C ENSP00000359662.2:p.Lys122Asn
ENST00000370629.6:c.429A>C ENSP00000359663.2:p.Lys143Asn
NM_000074.2:c.429A>C , LRG_141t1:c.429A>C NP_000065.1:p.Lys143Asn
NM_000074.3:c.429A>C MANE Select NP_000065.1:p.Lys143Asn