Canonical Allele Identifier: CA414757232

Gene: CD40LG

Linked Data

• gnomAD v4: X-136659411-T-C
• MyVariant Identifiers: chrX:g.135741570T>C (hg19) ; chrX:g.136659411T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659411T>C , CM000685.2:g.136659411T>C	GRCh38
NC_000023.10:g.135741570T>C , CM000685.1:g.135741570T>C	GRCh37
NC_000023.9:g.135569236T>C	NCBI36
NG_007280.1:g.16235T>C , LRG_141:g.16235T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*400T>C	ENSP00000512122.1:n.*400T>C
ENST00000695725.1:c.*337T>C	ENSP00000512123.1:n.*337T>C
ENST00000695726.1:n.2750T>C
ENST00000695729.1:n.3585T>C
ENST00000370629.7:c.782T>C MANE Select	ENSP00000359663.2:p.Leu261Pro
ENST00000370628.2:c.719T>C	ENSP00000359662.2:p.Leu240Pro
ENST00000370629.6:c.782T>C	ENSP00000359663.2:p.Leu261Pro
NM_000074.2:c.782T>C , LRG_141t1:c.782T>C	NP_000065.1:p.Leu261Pro
NM_000074.3:c.782T>C MANE Select	NP_000065.1:p.Leu261Pro