Canonical Allele Identifier: CA414752212
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648394G>C , CM000685.2:g.136648394G>C GRCh38
NC_000023.10:g.135730553G>C , CM000685.1:g.135730553G>C GRCh37
NC_000023.9:g.135558219G>C NCBI36
NG_007280.1:g.5218G>C , LRG_141:g.5218G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.146G>C ENSP00000512122.1:p.Arg49Thr
ENST00000695725.1:c.146G>C ENSP00000512123.1:p.Arg49Thr
ENST00000695726.1:n.189G>C
ENST00000695727.1:n.133G>C
ENST00000695728.1:n.133G>C
ENST00000370629.7:c.146G>C MANE Select ENSP00000359663.2:p.Arg49Thr
ENST00000370628.2:c.146G>C ENSP00000359662.2:p.Arg49Thr
ENST00000370629.6:c.146G>C ENSP00000359663.2:p.Arg49Thr
NM_000074.2:c.146G>C , LRG_141t1:c.146G>C NP_000065.1:p.Arg49Thr
NM_000074.3:c.146G>C MANE Select NP_000065.1:p.Arg49Thr