Canonical Allele Identifier: CA414756019
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659228G>C , CM000685.2:g.136659228G>C GRCh38
NC_000023.10:g.135741387G>C , CM000685.1:g.135741387G>C GRCh37
NC_000023.9:g.135569053G>C NCBI36
NG_007280.1:g.16052G>C , LRG_141:g.16052G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*217G>C ENSP00000512122.1:n.*217G>C
ENST00000695725.1:c.*154G>C ENSP00000512123.1:n.*154G>C
ENST00000695726.1:n.2567G>C
ENST00000695729.1:n.3402G>C
ENST00000370629.7:c.599G>C MANE Select ENSP00000359663.2:p.Arg200Thr
ENST00000370628.2:c.536G>C ENSP00000359662.2:p.Arg179Thr
ENST00000370629.6:c.599G>C ENSP00000359663.2:p.Arg200Thr
NM_000074.2:c.599G>C , LRG_141t1:c.599G>C NP_000065.1:p.Arg200Thr
NM_000074.3:c.599G>C MANE Select NP_000065.1:p.Arg200Thr