Canonical Allele Identifier: CA518856058

Gene: CD40LG

Linked Data

• ClinVar Variation Id: 2841571
• ClinVar RCV Id: RCV003623074
• gnomAD v4: X-136659349-T-C
• MyVariant Identifiers: chrX:g.135741508T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659349T>C , CM000685.2:g.136659349T>C	GRCh38
NC_000023.10:g.135741508T>C , CM000685.1:g.135741508T>C	GRCh37
NC_000023.9:g.135569174T>C	NCBI36
NG_007280.1:g.16173T>C , LRG_141:g.16173T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*338T>C	ENSP00000512122.1:n.*338T>C
ENST00000695725.1:c.*275T>C	ENSP00000512123.1:n.*275T>C
ENST00000695726.1:n.2688T>C
ENST00000695729.1:n.3523T>C
ENST00000370629.7:c.720T>C MANE Select	ENSP00000359663.2:p.Asn240=
ENST00000370628.2:c.657T>C	ENSP00000359662.2:p.Asn219=
ENST00000370629.6:c.720T>C	ENSP00000359663.2:p.Asn240=
NM_000074.2:c.720T>C , LRG_141t1:c.720T>C	NP_000065.1:p.Asn240=
NM_000074.3:c.720T>C MANE Select	NP_000065.1:p.Asn240=