Canonical Allele Identifier: CA414756564

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741479T>A (hg19) ; chrX:g.136659320T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659320T>A , CM000685.2:g.136659320T>A	GRCh38
NC_000023.10:g.135741479T>A , CM000685.1:g.135741479T>A	GRCh37
NC_000023.9:g.135569145T>A	NCBI36
NG_007280.1:g.16144T>A , LRG_141:g.16144T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*309T>A	ENSP00000512122.1:n.*309T>A
ENST00000695725.1:c.*246T>A	ENSP00000512123.1:n.*246T>A
ENST00000695726.1:n.2659T>A
ENST00000695729.1:n.3494T>A
ENST00000370629.7:c.691T>A MANE Select	ENSP00000359663.2:p.Leu231Met
ENST00000370628.2:c.628T>A	ENSP00000359662.2:p.Leu210Met
ENST00000370629.6:c.691T>A	ENSP00000359663.2:p.Leu231Met
NM_000074.2:c.691T>A , LRG_141t1:c.691T>A	NP_000065.1:p.Leu231Met
NM_000074.3:c.691T>A MANE Select	NP_000065.1:p.Leu231Met