Canonical Allele Identifier: CA414756286

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741427T>A (hg19) ; chrX:g.136659268T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659268T>A , CM000685.2:g.136659268T>A	GRCh38
NC_000023.10:g.135741427T>A , CM000685.1:g.135741427T>A	GRCh37
NC_000023.9:g.135569093T>A	NCBI36
NG_007280.1:g.16092T>A , LRG_141:g.16092T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*257T>A	ENSP00000512122.1:n.*257T>A
ENST00000695725.1:c.*194T>A	ENSP00000512123.1:n.*194T>A
ENST00000695726.1:n.2607T>A
ENST00000695729.1:n.3442T>A
ENST00000370629.7:c.639T>A MANE Select	ENSP00000359663.2:p.Ser213Arg
ENST00000370628.2:c.576T>A	ENSP00000359662.2:p.Ser192Arg
ENST00000370629.6:c.639T>A	ENSP00000359663.2:p.Ser213Arg
NM_000074.2:c.639T>A , LRG_141t1:c.639T>A	NP_000065.1:p.Ser213Arg
NM_000074.3:c.639T>A MANE Select	NP_000065.1:p.Ser213Arg