Canonical Allele Identifier: CA518856063

Gene: CD40LG

Linked Data

• dbSNP Id: rs1480516590
• gnomAD v2: X-135741514-T-C
• gnomAD v4: X-136659355-T-C
• MyVariant Identifiers: chrX:g.135741514T>C (hg19) ; chrX:g.136659355T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659355T>C , CM000685.2:g.136659355T>C	GRCh38
NC_000023.10:g.135741514T>C , CM000685.1:g.135741514T>C	GRCh37
NC_000023.9:g.135569180T>C	NCBI36
NG_007280.1:g.16179T>C , LRG_141:g.16179T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*344T>C	ENSP00000512122.1:n.*344T>C
ENST00000695725.1:c.*281T>C	ENSP00000512123.1:n.*281T>C
ENST00000695726.1:n.2694T>C
ENST00000695729.1:n.3529T>C
ENST00000370629.7:c.726T>C MANE Select	ENSP00000359663.2:p.Thr242=
ENST00000370628.2:c.663T>C	ENSP00000359662.2:p.Thr221=
ENST00000370629.6:c.726T>C	ENSP00000359663.2:p.Thr242=
NM_000074.2:c.726T>C , LRG_141t1:c.726T>C	NP_000065.1:p.Thr242=
NM_000074.3:c.726T>C MANE Select	NP_000065.1:p.Thr242=