Canonical Allele Identifier: CA336267472

Gene: CD40LG

Linked Data

• dbSNP Id: rs764969326
• gnomAD v2: X-135741529-G-A
• gnomAD v4: X-136659370-G-A
• MyVariant Identifiers: chrX:g.135741529G>A (hg19) ; chrX:g.136659370G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659370G>A , CM000685.2:g.136659370G>A	GRCh38
NC_000023.10:g.135741529G>A , CM000685.1:g.135741529G>A	GRCh37
NC_000023.9:g.135569195G>A	NCBI36
NG_007280.1:g.16194G>A , LRG_141:g.16194G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*359G>A	ENSP00000512122.1:n.*359G>A
ENST00000695725.1:c.*296G>A	ENSP00000512123.1:n.*296G>A
ENST00000695726.1:n.2709G>A
ENST00000695729.1:n.3544G>A
ENST00000370629.7:c.741G>A MANE Select	ENSP00000359663.2:p.Val247=
ENST00000370628.2:c.678G>A	ENSP00000359662.2:p.Val226=
ENST00000370629.6:c.741G>A	ENSP00000359663.2:p.Val247=
NM_000074.2:c.741G>A , LRG_141t1:c.741G>A	NP_000065.1:p.Val247=
NM_000074.3:c.741G>A MANE Select	NP_000065.1:p.Val247=