Canonical Allele Identifier: CA414755805

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135741312T>G (hg19) ; chrX:g.136659153T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659153T>G , CM000685.2:g.136659153T>G	GRCh38
NC_000023.10:g.135741312T>G , CM000685.1:g.135741312T>G	GRCh37
NC_000023.9:g.135568978T>G	NCBI36
NG_007280.1:g.15977T>G , LRG_141:g.15977T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*142T>G	ENSP00000512122.1:n.*142T>G
ENST00000695725.1:c.*79T>G	ENSP00000512123.1:n.*79T>G
ENST00000695726.1:n.2492T>G
ENST00000695729.1:n.3327T>G
ENST00000370629.7:c.524T>G MANE Select	ENSP00000359663.2:p.Val175Gly
ENST00000370628.2:c.461T>G	ENSP00000359662.2:p.Val154Gly
ENST00000370629.6:c.524T>G	ENSP00000359663.2:p.Val175Gly
NM_000074.2:c.524T>G , LRG_141t1:c.524T>G	NP_000065.1:p.Val175Gly
NM_000074.3:c.524T>G MANE Select	NP_000065.1:p.Val175Gly