Canonical Allele Identifier: CA518856023
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741454C>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659295C>A , CM000685.2:g.136659295C>A GRCh38
NC_000023.10:g.135741454C>A , CM000685.1:g.135741454C>A GRCh37
NC_000023.9:g.135569120C>A NCBI36
NG_007280.1:g.16119C>A , LRG_141:g.16119C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*284C>A ENSP00000512122.1:n.*284C>A
ENST00000695725.1:c.*221C>A ENSP00000512123.1:n.*221C>A
ENST00000695726.1:n.2634C>A
ENST00000695729.1:n.3469C>A
ENST00000370629.7:c.666C>A MANE Select ENSP00000359663.2:p.Ser222=
ENST00000370628.2:c.603C>A ENSP00000359662.2:p.Ser201=
ENST00000370629.6:c.666C>A ENSP00000359663.2:p.Ser222=
NM_000074.2:c.666C>A , LRG_141t1:c.666C>A NP_000065.1:p.Ser222=
NM_000074.3:c.666C>A MANE Select NP_000065.1:p.Ser222=
Search 100 bp 5'
Search 100 bp 3'