Canonical Allele Identifier: CA518855815
Gene: CD40LG HGNC NCBI

Linked Data

gnomAD v4: X-136659055-A-G
MyVariant Identifiers: chrX:g.135741214A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659055A>G , CM000685.2:g.136659055A>G GRCh38
NC_000023.10:g.135741214A>G , CM000685.1:g.135741214A>G GRCh37
NC_000023.9:g.135568880A>G NCBI36
NG_007280.1:g.15879A>G , LRG_141:g.15879A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*44A>G ENSP00000512122.1:n.*44A>G
ENST00000695725.1:c.173A>G ENSP00000512123.1:p.Lys58Arg
ENST00000695726.1:n.2394A>G
ENST00000695729.1:n.3229A>G
ENST00000370629.7:c.426A>G MANE Select ENSP00000359663.2:p.Glu142=
ENST00000370628.2:c.363A>G ENSP00000359662.2:p.Glu121=
ENST00000370629.6:c.426A>G ENSP00000359663.2:p.Glu142=
NM_000074.2:c.426A>G , LRG_141t1:c.426A>G NP_000065.1:p.Glu142=
NM_000074.3:c.426A>G MANE Select NP_000065.1:p.Glu142=
Search 100 bp 5'
Search 100 bp 3'