Canonical Allele Identifier: CA10528163
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs374246579

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659229A>C , CM000685.2:g.136659229A>C GRCh38
NC_000023.10:g.135741388A>C , CM000685.1:g.135741388A>C GRCh37
NC_000023.9:g.135569054A>C NCBI36
NG_007280.1:g.16053A>C , LRG_141:g.16053A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*218A>C ENSP00000512122.1:n.*218A>C
ENST00000695725.1:c.*155A>C ENSP00000512123.1:n.*155A>C
ENST00000695726.1:n.2568A>C
ENST00000695729.1:n.3403A>C
ENST00000370629.7:c.600A>C MANE Select ENSP00000359663.2:p.Arg200Ser
ENST00000370628.2:c.537A>C ENSP00000359662.2:p.Arg179Ser
ENST00000370629.6:c.600A>C ENSP00000359663.2:p.Arg200Ser
NM_000074.2:c.600A>C , LRG_141t1:c.600A>C NP_000065.1:p.Arg200Ser
NM_000074.3:c.600A>C MANE Select NP_000065.1:p.Arg200Ser