Canonical Allele Identifier: CA336267431

Gene: CD40LG

Linked Data

• dbSNP Id: rs1008743849
• MyVariant Identifiers: chrX:g.135741356A>G (hg19) ; chrX:g.136659197A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659197A>G , CM000685.2:g.136659197A>G	GRCh38
NC_000023.10:g.135741356A>G , CM000685.1:g.135741356A>G	GRCh37
NC_000023.9:g.135569022A>G	NCBI36
NG_007280.1:g.16021A>G , LRG_141:g.16021A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*186A>G	ENSP00000512122.1:n.*186A>G
ENST00000695725.1:c.*123A>G	ENSP00000512123.1:n.*123A>G
ENST00000695726.1:n.2536A>G
ENST00000695729.1:n.3371A>G
ENST00000370629.7:c.568A>G MANE Select	ENSP00000359663.2:p.Ile190Val
ENST00000370628.2:c.505A>G	ENSP00000359662.2:p.Ile169Val
ENST00000370629.6:c.568A>G	ENSP00000359663.2:p.Ile190Val
NM_000074.2:c.568A>G , LRG_141t1:c.568A>G	NP_000065.1:p.Ile190Val
NM_000074.3:c.568A>G MANE Select	NP_000065.1:p.Ile190Val