Canonical Allele Identifier: CA414755552

Gene: CD40LG

Linked Data

• gnomAD v4: X-136659039-T-A
• MyVariant Identifiers: chrX:g.135741198T>A (hg19) ; chrX:g.136659039T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659039T>A , CM000685.2:g.136659039T>A	GRCh38
NC_000023.10:g.135741198T>A , CM000685.1:g.135741198T>A	GRCh37
NC_000023.9:g.135568864T>A	NCBI36
NG_007280.1:g.15863T>A , LRG_141:g.15863T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*28T>A	ENSP00000512122.1:n.*28T>A
ENST00000695725.1:c.157T>A	ENSP00000512123.1:p.Cys53Ser
ENST00000695726.1:n.2378T>A
ENST00000695729.1:n.3213T>A
ENST00000370629.7:c.410T>A MANE Select	ENSP00000359663.2:p.Val137Glu
ENST00000370628.2:c.347T>A	ENSP00000359662.2:p.Val116Glu
ENST00000370629.6:c.410T>A	ENSP00000359663.2:p.Val137Glu
NM_000074.2:c.410T>A , LRG_141t1:c.410T>A	NP_000065.1:p.Val137Glu
NM_000074.3:c.410T>A MANE Select	NP_000065.1:p.Val137Glu