Canonical Allele Identifier: CA414755726

Gene: CD40LG

Linked Data

• gnomAD v4: X-136659119-A-G
• MyVariant Identifiers: chrX:g.135741278A>G (hg19) ; chrX:g.136659119A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659119A>G , CM000685.2:g.136659119A>G	GRCh38
NC_000023.10:g.135741278A>G , CM000685.1:g.135741278A>G	GRCh37
NC_000023.9:g.135568944A>G	NCBI36
NG_007280.1:g.15943A>G , LRG_141:g.15943A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*108A>G	ENSP00000512122.1:n.*108A>G
ENST00000695725.1:c.*45A>G	ENSP00000512123.1:n.*45A>G
ENST00000695726.1:n.2458A>G
ENST00000695729.1:n.3293A>G
ENST00000370629.7:c.490A>G MANE Select	ENSP00000359663.2:p.Lys164Glu
ENST00000370628.2:c.427A>G	ENSP00000359662.2:p.Lys143Glu
ENST00000370629.6:c.490A>G	ENSP00000359663.2:p.Lys164Glu
NM_000074.2:c.490A>G , LRG_141t1:c.490A>G	NP_000065.1:p.Lys164Glu
NM_000074.3:c.490A>G MANE Select	NP_000065.1:p.Lys164Glu