Canonical Allele Identifier: CA414756369

Gene: CD40LG

Linked Data

• ClinVar Variation Id: 660932
• ClinVar RCV Id: RCV000818235
• dbSNP Id: rs1603321834
• MyVariant Identifiers: chrX:g.135741449C>T (hg19) ; chrX:g.136659290C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659290C>T , CM000685.2:g.136659290C>T	GRCh38
NC_000023.10:g.135741449C>T , CM000685.1:g.135741449C>T	GRCh37
NC_000023.9:g.135569115C>T	NCBI36
NG_007280.1:g.16114C>T , LRG_141:g.16114C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000695724.1:c.*279C>T	ENSP00000512122.1:n.*279C>T
ENST00000695725.1:c.*216C>T	ENSP00000512123.1:n.*216C>T
ENST00000695726.1:n.2629C>T
ENST00000695729.1:n.3464C>T
ENST00000370629.7:c.661C>T MANE Select	ENSP00000359663.2:p.Gln221Ter
ENST00000370628.2:c.598C>T	ENSP00000359662.2:p.Gln200Ter
ENST00000370629.6:c.661C>T	ENSP00000359663.2:p.Gln221Ter
NM_000074.2:c.661C>T , LRG_141t1:c.661C>T	NP_000065.1:p.Gln221Ter
NM_000074.3:c.661C>T MANE Select	NP_000065.1:p.Gln221Ter