Canonical Allele Identifier: CA518856079
Gene: CD40LG HGNC NCBI

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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