Canonical Allele Identifier: CA414752228

Gene: CD40LG

Linked Data

• gnomAD v4: X-136648401-C-A
• MyVariant Identifiers: chrX:g.135730560C>A (hg19) ; chrX:g.136648401C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648401C>A , CM000685.2:g.136648401C>A	GRCh38
NC_000023.10:g.135730560C>A , CM000685.1:g.135730560C>A	GRCh37
NC_000023.9:g.135558226C>A	NCBI36
NG_007280.1:g.5225C>A , LRG_141:g.5225C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.153C>A	ENSP00000512122.1:p.Asp51Glu
ENST00000695725.1:c.153C>A	ENSP00000512123.1:p.Asp51Glu
ENST00000695726.1:n.196C>A
ENST00000695727.1:n.140C>A
ENST00000695728.1:n.140C>A
ENST00000370629.7:c.153C>A MANE Select	ENSP00000359663.2:p.Asp51Glu
ENST00000370628.2:c.153C>A	ENSP00000359662.2:p.Asp51Glu
ENST00000370629.6:c.153C>A	ENSP00000359663.2:p.Asp51Glu
NM_000074.2:c.153C>A , LRG_141t1:c.153C>A	NP_000065.1:p.Asp51Glu
NM_000074.3:c.153C>A MANE Select	NP_000065.1:p.Asp51Glu