Canonical Allele Identifier: CA414755919

Gene: CD40LG

Linked Data

• gnomAD v4: X-136659205-C-G
• MyVariant Identifiers: chrX:g.135741364C>G (hg19) ; chrX:g.136659205C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659205C>G , CM000685.2:g.136659205C>G	GRCh38
NC_000023.10:g.135741364C>G , CM000685.1:g.135741364C>G	GRCh37
NC_000023.9:g.135569030C>G	NCBI36
NG_007280.1:g.16029C>G , LRG_141:g.16029C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*194C>G	ENSP00000512122.1:n.*194C>G
ENST00000695725.1:c.*131C>G	ENSP00000512123.1:n.*131C>G
ENST00000695726.1:n.2544C>G
ENST00000695729.1:n.3379C>G
ENST00000370629.7:c.576C>G MANE Select	ENSP00000359663.2:p.Ser192Arg
ENST00000370628.2:c.513C>G	ENSP00000359662.2:p.Ser171Arg
ENST00000370629.6:c.576C>G	ENSP00000359663.2:p.Ser192Arg
NM_000074.2:c.576C>G , LRG_141t1:c.576C>G	NP_000065.1:p.Ser192Arg
NM_000074.3:c.576C>G MANE Select	NP_000065.1:p.Ser192Arg