Canonical Allele Identifier: CA518779101
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135730440A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648281A>C , CM000685.2:g.136648281A>C GRCh38
NC_000023.10:g.135730440A>C , CM000685.1:g.135730440A>C GRCh37
NC_000023.9:g.135558106A>C NCBI36
NG_007280.1:g.5105A>C , LRG_141:g.5105A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.33A>C ENSP00000512122.1:p.Arg11=
ENST00000695725.1:c.33A>C ENSP00000512123.1:p.Arg11=
ENST00000695726.1:n.76A>C
ENST00000695727.1:n.20A>C
ENST00000695728.1:n.20A>C
ENST00000370629.7:c.33A>C MANE Select ENSP00000359663.2:p.Arg11=
ENST00000370628.2:c.33A>C ENSP00000359662.2:p.Arg11=
ENST00000370629.6:c.33A>C ENSP00000359663.2:p.Arg11=
NM_000074.2:c.33A>C , LRG_141t1:c.33A>C NP_000065.1:p.Arg11=
NM_000074.3:c.33A>C MANE Select NP_000065.1:p.Arg11=
Search 100 bp 5'
Search 100 bp 3'