Canonical Allele Identifier: CA414756291

Gene: CD40LG

Linked Data

• dbSNP Id: rs2148553759
• MyVariant Identifiers: chrX:g.135741428T>A (hg19) ; chrX:g.136659269T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659269T>A , CM000685.2:g.136659269T>A	GRCh38
NC_000023.10:g.135741428T>A , CM000685.1:g.135741428T>A	GRCh37
NC_000023.9:g.135569094T>A	NCBI36
NG_007280.1:g.16093T>A , LRG_141:g.16093T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*258T>A	ENSP00000512122.1:n.*258T>A
ENST00000695725.1:c.*195T>A	ENSP00000512123.1:n.*195T>A
ENST00000695726.1:n.2608T>A
ENST00000695729.1:n.3443T>A
ENST00000370629.7:c.640T>A MANE Select	ENSP00000359663.2:p.Ser214Thr
ENST00000370628.2:c.577T>A	ENSP00000359662.2:p.Ser193Thr
ENST00000370629.6:c.640T>A	ENSP00000359663.2:p.Ser214Thr
NM_000074.2:c.640T>A , LRG_141t1:c.640T>A	NP_000065.1:p.Ser214Thr
NM_000074.3:c.640T>A MANE Select	NP_000065.1:p.Ser214Thr