Canonical Allele Identifier: CA645125313

Gene: CD40LG

Linked Data

• dbSNP Id: rs1326915541
• gnomAD v2: X-135741072-A-G
• gnomAD v3: X-136658913-A-G
• gnomAD v4: X-136658913-A-G
• MyVariant Identifiers: chrX:g.135741072A>G (hg19) ; chrX:g.136658913A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136658913A>G , CM000685.2:g.136658913A>G	GRCh38
NC_000023.10:g.135741072A>G , CM000685.1:g.135741072A>G	GRCh37
NC_000023.9:g.135568738A>G	NCBI36
NG_007280.1:g.15737A>G , LRG_141:g.15737A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*28-126A>G	ENSP00000512122.1:n.*28-126A>G
ENST00000695725.1:c.157-126A>G	ENSP00000512123.1:n.157-126A>G
ENST00000695726.1:n.2378-126A>G
ENST00000695729.1:n.3213-126A>G
ENST00000370629.7:c.410-126A>G MANE Select	ENSP00000359663.2:n.410-126A>G
ENST00000370628.2:c.347-126A>G	ENSP00000359662.2:n.347-126A>G
ENST00000370629.6:c.410-126A>G	ENSP00000359663.2:n.410-126A>G
NM_000074.2:c.410-126A>G , LRG_141t1:c.410-126A>G	NP_000065.1:n.410-126A>G
NM_000074.3:c.410-126A>G MANE Select	NP_000065.1:n.410-126A>G