Canonical Allele Identifier: CA10528142
Gene: CD40LG HGNC NCBI

Linked Data

ClinVar Variation Id: 518407
ClinVar RCV Id: RCV001619808 RCV003488729
dbSNP Id: rs3092923
ExAC: X:135741185 T / C
gnomAD v2: X-135741185-T-C
gnomAD v3: X-136659026-T-C
gnomAD v4: X-136659026-T-C
MyVariant Identifiers: chrX:g.135741185T>C (hg19) chrX:g.136659026T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659026T>C , CM000685.2:g.136659026T>C GRCh38
NC_000023.10:g.135741185T>C , CM000685.1:g.135741185T>C GRCh37
NC_000023.9:g.135568851T>C NCBI36
NG_007280.1:g.15850T>C , LRG_141:g.15850T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*28-13T>C ENSP00000512122.1:n.*28-13T>C
ENST00000695725.1:c.157-13T>C ENSP00000512123.1:n.157-13T>C
ENST00000695726.1:n.2378-13T>C
ENST00000695729.1:n.3213-13T>C
ENST00000370629.7:c.410-13T>C MANE Select ENSP00000359663.2:n.410-13T>C
ENST00000370628.2:c.347-13T>C ENSP00000359662.2:n.347-13T>C
ENST00000370629.6:c.410-13T>C ENSP00000359663.2:n.410-13T>C
NM_000074.2:c.410-13T>C , LRG_141t1:c.410-13T>C NP_000065.1:n.410-13T>C
NM_000074.3:c.410-13T>C MANE Select NP_000065.1:n.410-13T>C
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