Canonical Allele Identifier: CA414756460

Gene: CD40LG

Linked Data

• COSMIC: COSM3231691
• MyVariant Identifiers: chrX:g.135741465G>A (hg19) ; chrX:g.136659306G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659306G>A , CM000685.2:g.136659306G>A	GRCh38
NC_000023.10:g.135741465G>A , CM000685.1:g.135741465G>A	GRCh37
NC_000023.9:g.135569131G>A	NCBI36
NG_007280.1:g.16130G>A , LRG_141:g.16130G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*295G>A	ENSP00000512122.1:n.*295G>A
ENST00000695725.1:c.*232G>A	ENSP00000512123.1:n.*232G>A
ENST00000695726.1:n.2645G>A
ENST00000695729.1:n.3480G>A
ENST00000370629.7:c.677G>A MANE Select	ENSP00000359663.2:p.Gly226Glu
ENST00000370628.2:c.614G>A	ENSP00000359662.2:p.Gly205Glu
ENST00000370629.6:c.677G>A	ENSP00000359663.2:p.Gly226Glu
NM_000074.2:c.677G>A , LRG_141t1:c.677G>A	NP_000065.1:p.Gly226Glu
NM_000074.3:c.677G>A MANE Select	NP_000065.1:p.Gly226Glu