Canonical Allele Identifier: CA518855941

Gene: CD40LG

Linked Data

• gnomAD v4: X-136659172-G-A
• MyVariant Identifiers: chrX:g.135741331G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659172G>A , CM000685.2:g.136659172G>A	GRCh38
NC_000023.10:g.135741331G>A , CM000685.1:g.135741331G>A	GRCh37
NC_000023.9:g.135568997G>A	NCBI36
NG_007280.1:g.15996G>A , LRG_141:g.15996G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*161G>A	ENSP00000512122.1:n.*161G>A
ENST00000695725.1:c.*98G>A	ENSP00000512123.1:n.*98G>A
ENST00000695726.1:n.2511G>A
ENST00000695729.1:n.3346G>A
ENST00000370629.7:c.543G>A MANE Select	ENSP00000359663.2:p.Arg181=
ENST00000370628.2:c.480G>A	ENSP00000359662.2:p.Arg160=
ENST00000370629.6:c.543G>A	ENSP00000359663.2:p.Arg181=
NM_000074.2:c.543G>A , LRG_141t1:c.543G>A	NP_000065.1:p.Arg181=
NM_000074.3:c.543G>A MANE Select	NP_000065.1:p.Arg181=