Canonical Allele Identifier: CA414756924

Gene: CD40LG

Linked Data

• dbSNP Id: rs2076128005
• MyVariant Identifiers: chrX:g.135741527G>A (hg19) ; chrX:g.136659368G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659368G>A , CM000685.2:g.136659368G>A	GRCh38
NC_000023.10:g.135741527G>A , CM000685.1:g.135741527G>A	GRCh37
NC_000023.9:g.135569193G>A	NCBI36
NG_007280.1:g.16192G>A , LRG_141:g.16192G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*357G>A	ENSP00000512122.1:n.*357G>A
ENST00000695725.1:c.*294G>A	ENSP00000512123.1:n.*294G>A
ENST00000695726.1:n.2707G>A
ENST00000695729.1:n.3542G>A
ENST00000370629.7:c.739G>A MANE Select	ENSP00000359663.2:p.Val247Met
ENST00000370628.2:c.676G>A	ENSP00000359662.2:p.Val226Met
ENST00000370629.6:c.739G>A	ENSP00000359663.2:p.Val247Met
NM_000074.2:c.739G>A , LRG_141t1:c.739G>A	NP_000065.1:p.Val247Met
NM_000074.3:c.739G>A MANE Select	NP_000065.1:p.Val247Met