Canonical Allele Identifier: CA414753468

Gene: CD40LG

Linked Data

• ClinVar Variation Id: 439469
• ClinVar RCV Id: RCV000508287
• dbSNP Id: rs1556136676
• MyVariant Identifiers: chrX:g.135732524G>A (hg19) ; chrX:g.136650365G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136650365G>A , CM000685.2:g.136650365G>A	GRCh38
NC_000023.10:g.135732524G>A , CM000685.1:g.135732524G>A	GRCh37
NC_000023.9:g.135560190G>A	NCBI36
NG_007280.1:g.7189G>A , LRG_141:g.7189G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.256G>A	ENSP00000512122.1:p.Glu86Lys
ENST00000695725.1:c.156+1961G>A	ENSP00000512123.1:n.156+1961G>A
ENST00000695726.1:n.299G>A
ENST00000695727.1:n.243G>A
ENST00000695728.1:n.243G>A
ENST00000370629.7:c.256G>A MANE Select	ENSP00000359663.2:p.Glu86Lys
ENST00000370628.2:c.256G>A	ENSP00000359662.2:p.Glu86Lys
ENST00000370629.6:c.256G>A	ENSP00000359663.2:p.Glu86Lys
NM_000074.2:c.256G>A , LRG_141t1:c.256G>A	NP_000065.1:p.Glu86Lys
NM_000074.3:c.256G>A MANE Select	NP_000065.1:p.Glu86Lys