Canonical Allele Identifier: CA414756682

Gene: CD40LG

Linked Data

• gnomAD v4: X-136659336-C-G
• MyVariant Identifiers: chrX:g.135741495C>G (hg19) ; chrX:g.136659336C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659336C>G , CM000685.2:g.136659336C>G	GRCh38
NC_000023.10:g.135741495C>G , CM000685.1:g.135741495C>G	GRCh37
NC_000023.9:g.135569161C>G	NCBI36
NG_007280.1:g.16160C>G , LRG_141:g.16160C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*325C>G	ENSP00000512122.1:n.*325C>G
ENST00000695725.1:c.*262C>G	ENSP00000512123.1:n.*262C>G
ENST00000695726.1:n.2675C>G
ENST00000695729.1:n.3510C>G
ENST00000370629.7:c.707C>G MANE Select	ENSP00000359663.2:p.Ser236Trp
ENST00000370628.2:c.644C>G	ENSP00000359662.2:p.Ser215Trp
ENST00000370629.6:c.707C>G	ENSP00000359663.2:p.Ser236Trp
NM_000074.2:c.707C>G , LRG_141t1:c.707C>G	NP_000065.1:p.Ser236Trp
NM_000074.3:c.707C>G MANE Select	NP_000065.1:p.Ser236Trp