Canonical Allele Identifier: CA518855875

Gene: CD40LG

Linked Data

• gnomAD v4: X-136659115-C-A
• MyVariant Identifiers: chrX:g.135741274C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659115C>A , CM000685.2:g.136659115C>A	GRCh38
NC_000023.10:g.135741274C>A , CM000685.1:g.135741274C>A	GRCh37
NC_000023.9:g.135568940C>A	NCBI36
NG_007280.1:g.15939C>A , LRG_141:g.15939C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*104C>A	ENSP00000512122.1:n.*104C>A
ENST00000695725.1:c.*41C>A	ENSP00000512123.1:n.*41C>A
ENST00000695726.1:n.2454C>A
ENST00000695729.1:n.3289C>A
ENST00000370629.7:c.486C>A MANE Select	ENSP00000359663.2:p.Thr162=
ENST00000370628.2:c.423C>A	ENSP00000359662.2:p.Thr141=
ENST00000370629.6:c.486C>A	ENSP00000359663.2:p.Thr162=
NM_000074.2:c.486C>A , LRG_141t1:c.486C>A	NP_000065.1:p.Thr162=
NM_000074.3:c.486C>A MANE Select	NP_000065.1:p.Thr162=