Canonical Allele Identifier: CA414751469

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135730432T>A (hg19) ; chrX:g.136648273T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648273T>A , CM000685.2:g.136648273T>A	GRCh38
NC_000023.10:g.135730432T>A , CM000685.1:g.135730432T>A	GRCh37
NC_000023.9:g.135558098T>A	NCBI36
NG_007280.1:g.5097T>A , LRG_141:g.5097T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.25T>A	ENSP00000512122.1:p.Ser9Thr
ENST00000695725.1:c.25T>A	ENSP00000512123.1:p.Ser9Thr
ENST00000695726.1:n.68T>A
ENST00000695727.1:n.12T>A
ENST00000695728.1:n.12T>A
ENST00000370629.7:c.25T>A MANE Select	ENSP00000359663.2:p.Ser9Thr
ENST00000370628.2:c.25T>A	ENSP00000359662.2:p.Ser9Thr
ENST00000370629.6:c.25T>A	ENSP00000359663.2:p.Ser9Thr
NM_000074.2:c.25T>A , LRG_141t1:c.25T>A	NP_000065.1:p.Ser9Thr
NM_000074.3:c.25T>A MANE Select	NP_000065.1:p.Ser9Thr