Canonical Allele Identifier: CA871926147

Gene: CD40LG

Linked Data

• ClinVar Variation Id: 2834744
• ClinVar RCV Id: RCV003622964
• dbSNP Id: rs1424339099
• gnomAD v3: X-136648411-T-A
• gnomAD v4: X-136648411-T-A
• MyVariant Identifiers: chrX:g.135730570T>A (hg19) ; chrX:g.136648411T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648411T>A , CM000685.2:g.136648411T>A	GRCh38
NC_000023.10:g.135730570T>A , CM000685.1:g.135730570T>A	GRCh37
NC_000023.9:g.135558236T>A	NCBI36
NG_007280.1:g.5235T>A , LRG_141:g.5235T>A

Transcript Alleles

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