Canonical Allele Identifier: CA10528076
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 1169084
ClinVar RCV Id: RCV001519876
dbSNP Id: rs755782893
ExAC: X:135730580 G / A
gnomAD v2: X-135730580-G-A
gnomAD v3: X-136648421-G-A
gnomAD v4: X-136648421-G-A
MyVariant Identifiers: chrX:g.135730580G>A (hg19) chrX:g.136648421G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648421G>A , CM000685.2:g.136648421G>A GRCh38
NC_000023.10:g.135730580G>A , CM000685.1:g.135730580G>A GRCh37
NC_000023.9:g.135558246G>A NCBI36
NG_007280.1:g.5245G>A , LRG_141:g.5245G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.156+17G>A ENSP00000512122.1:n.156+17G>A
ENST00000695725.1:c.156+17G>A ENSP00000512123.1:n.156+17G>A
ENST00000695726.1:n.199+17G>A
ENST00000695727.1:n.143+17G>A
ENST00000695728.1:n.143+17G>A
ENST00000370629.7:c.156+17G>A MANE Select ENSP00000359663.2:n.156+17G>A
ENST00000370628.2:c.156+17G>A ENSP00000359662.2:n.156+17G>A
ENST00000370629.6:c.156+17G>A ENSP00000359663.2:n.156+17G>A
NM_000074.2:c.156+17G>A , LRG_141t1:c.156+17G>A NP_000065.1:n.156+17G>A
NM_000074.3:c.156+17G>A MANE Select NP_000065.1:n.156+17G>A
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