Canonical Allele Identifier: CA10528157
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 715352
ClinVar RCV Id: RCV000887806
dbSNP Id: rs147340102
ExAC: X:135741338 T / A
gnomAD v2: X-135741338-T-A
gnomAD v3: X-136659179-T-A
gnomAD v4: X-136659179-T-A
MyVariant Identifiers: chrX:g.135741338T>A (hg19) chrX:g.136659179T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659179T>A , CM000685.2:g.136659179T>A GRCh38
NC_000023.10:g.135741338T>A , CM000685.1:g.135741338T>A GRCh37
NC_000023.9:g.135569004T>A NCBI36
NG_007280.1:g.16003T>A , LRG_141:g.16003T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*168T>A ENSP00000512122.1:n.*168T>A
ENST00000695725.1:c.*105T>A ENSP00000512123.1:n.*105T>A
ENST00000695726.1:n.2518T>A
ENST00000695729.1:n.3353T>A
ENST00000370629.7:c.550T>A MANE Select ENSP00000359663.2:p.Ser184Thr
ENST00000370628.2:c.487T>A ENSP00000359662.2:p.Ser163Thr
ENST00000370629.6:c.550T>A ENSP00000359663.2:p.Ser184Thr
NM_000074.2:c.550T>A , LRG_141t1:c.550T>A NP_000065.1:p.Ser184Thr
NM_000074.3:c.550T>A MANE Select NP_000065.1:p.Ser184Thr
Search 100 bp 5'
Search 100 bp 3'