Canonical Allele Identifier: CA414756839

Gene: CD40LG

Linked Data

• COSMIC: COSM1715614
• MyVariant Identifiers: chrX:g.135741515G>A (hg19) ; chrX:g.136659356G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659356G>A , CM000685.2:g.136659356G>A	GRCh38
NC_000023.10:g.135741515G>A , CM000685.1:g.135741515G>A	GRCh37
NC_000023.9:g.135569181G>A	NCBI36
NG_007280.1:g.16180G>A , LRG_141:g.16180G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*345G>A	ENSP00000512122.1:n.*345G>A
ENST00000695725.1:c.*282G>A	ENSP00000512123.1:n.*282G>A
ENST00000695726.1:n.2695G>A
ENST00000695729.1:n.3530G>A
ENST00000370629.7:c.727G>A MANE Select	ENSP00000359663.2:p.Asp243Asn
ENST00000370628.2:c.664G>A	ENSP00000359662.2:p.Asp222Asn
ENST00000370629.6:c.727G>A	ENSP00000359663.2:p.Asp243Asn
NM_000074.2:c.727G>A , LRG_141t1:c.727G>A	NP_000065.1:p.Asp243Asn
NM_000074.3:c.727G>A MANE Select	NP_000065.1:p.Asp243Asn