Canonical Allele Identifier: CA414757120

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741554T>A (hg19) ; chrX:g.136659395T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659395T>A , CM000685.2:g.136659395T>A	GRCh38
NC_000023.10:g.135741554T>A , CM000685.1:g.135741554T>A	GRCh37
NC_000023.9:g.135569220T>A	NCBI36
NG_007280.1:g.16219T>A , LRG_141:g.16219T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*384T>A	ENSP00000512122.1:n.*384T>A
ENST00000695725.1:c.*321T>A	ENSP00000512123.1:n.*321T>A
ENST00000695726.1:n.2734T>A
ENST00000695729.1:n.3569T>A
ENST00000370629.7:c.766T>A MANE Select	ENSP00000359663.2:p.Phe256Ile
ENST00000370628.2:c.703T>A	ENSP00000359662.2:p.Phe235Ile
ENST00000370629.6:c.766T>A	ENSP00000359663.2:p.Phe256Ile
NM_000074.2:c.766T>A , LRG_141t1:c.766T>A	NP_000065.1:p.Phe256Ile
NM_000074.3:c.766T>A MANE Select	NP_000065.1:p.Phe256Ile