Canonical Allele Identifier: CA518856078
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741541T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659382T>C , CM000685.2:g.136659382T>C GRCh38
NC_000023.10:g.135741541T>C , CM000685.1:g.135741541T>C GRCh37
NC_000023.9:g.135569207T>C NCBI36
NG_007280.1:g.16206T>C , LRG_141:g.16206T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*371T>C ENSP00000512122.1:n.*371T>C
ENST00000695725.1:c.*308T>C ENSP00000512123.1:n.*308T>C
ENST00000695726.1:n.2721T>C
ENST00000695729.1:n.3556T>C
ENST00000370629.7:c.753T>C MANE Select ENSP00000359663.2:p.Thr251=
ENST00000370628.2:c.690T>C ENSP00000359662.2:p.Thr230=
ENST00000370629.6:c.753T>C ENSP00000359663.2:p.Thr251=
NM_000074.2:c.753T>C , LRG_141t1:c.753T>C NP_000065.1:p.Thr251=
NM_000074.3:c.753T>C MANE Select NP_000065.1:p.Thr251=