Canonical Allele Identifier: CA414751468

Gene: CD40LG

Linked Data

• MyVariant Identifiers: chrX:g.135730430C>G (hg19) ; chrX:g.136648271C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648271C>G , CM000685.2:g.136648271C>G	GRCh38
NC_000023.10:g.135730430C>G , CM000685.1:g.135730430C>G	GRCh37
NC_000023.9:g.135558096C>G	NCBI36
NG_007280.1:g.5095C>G , LRG_141:g.5095C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.23C>G	ENSP00000512122.1:p.Thr8Ser
ENST00000695725.1:c.23C>G	ENSP00000512123.1:p.Thr8Ser
ENST00000695726.1:n.66C>G
ENST00000695727.1:n.10C>G
ENST00000695728.1:n.10C>G
ENST00000370629.7:c.23C>G MANE Select	ENSP00000359663.2:p.Thr8Ser
ENST00000370628.2:c.23C>G	ENSP00000359662.2:p.Thr8Ser
ENST00000370629.6:c.23C>G	ENSP00000359663.2:p.Thr8Ser
NM_000074.2:c.23C>G , LRG_141t1:c.23C>G	NP_000065.1:p.Thr8Ser
NM_000074.3:c.23C>G MANE Select	NP_000065.1:p.Thr8Ser