Canonical Allele Identifier: CA518856077

Gene: CD40LG

Linked Data

• ClinVar Variation Id: 2790886
• ClinVar RCV Id: RCV003621901
• MyVariant Identifiers: chrX:g.135741541T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659382T>A , CM000685.2:g.136659382T>A	GRCh38
NC_000023.10:g.135741541T>A , CM000685.1:g.135741541T>A	GRCh37
NC_000023.9:g.135569207T>A	NCBI36
NG_007280.1:g.16206T>A , LRG_141:g.16206T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*371T>A	ENSP00000512122.1:n.*371T>A
ENST00000695725.1:c.*308T>A	ENSP00000512123.1:n.*308T>A
ENST00000695726.1:n.2721T>A
ENST00000695729.1:n.3556T>A
ENST00000370629.7:c.753T>A MANE Select	ENSP00000359663.2:p.Thr251=
ENST00000370628.2:c.690T>A	ENSP00000359662.2:p.Thr230=
ENST00000370629.6:c.753T>A	ENSP00000359663.2:p.Thr251=
NM_000074.2:c.753T>A , LRG_141t1:c.753T>A	NP_000065.1:p.Thr251=
NM_000074.3:c.753T>A MANE Select	NP_000065.1:p.Thr251=