Canonical Allele Identifier: CA518856081
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741544C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659385C>G , CM000685.2:g.136659385C>G GRCh38
NC_000023.10:g.135741544C>G , CM000685.1:g.135741544C>G GRCh37
NC_000023.9:g.135569210C>G NCBI36
NG_007280.1:g.16209C>G , LRG_141:g.16209C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*374C>G ENSP00000512122.1:n.*374C>G
ENST00000695725.1:c.*311C>G ENSP00000512123.1:n.*311C>G
ENST00000695726.1:n.2724C>G
ENST00000695729.1:n.3559C>G
ENST00000370629.7:c.756C>G MANE Select ENSP00000359663.2:p.Gly252=
ENST00000370628.2:c.693C>G ENSP00000359662.2:p.Gly231=
ENST00000370629.6:c.756C>G ENSP00000359663.2:p.Gly252=
NM_000074.2:c.756C>G , LRG_141t1:c.756C>G NP_000065.1:p.Gly252=
NM_000074.3:c.756C>G MANE Select NP_000065.1:p.Gly252=