Canonical Allele Identifier: CA518782419
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741571C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659412C>T , CM000685.2:g.136659412C>T GRCh38
NC_000023.10:g.135741571C>T , CM000685.1:g.135741571C>T GRCh37
NC_000023.9:g.135569237C>T NCBI36
NG_007280.1:g.16236C>T , LRG_141:g.16236C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*401C>T ENSP00000512122.1:n.*401C>T
ENST00000695725.1:c.*338C>T ENSP00000512123.1:n.*338C>T
ENST00000695726.1:n.2751C>T
ENST00000695729.1:n.3586C>T
ENST00000370629.7:c.783C>T MANE Select ENSP00000359663.2:p.Leu261=
ENST00000370628.2:c.720C>T ENSP00000359662.2:p.Leu240=
ENST00000370629.6:c.783C>T ENSP00000359663.2:p.Leu261=
NM_000074.2:c.783C>T , LRG_141t1:c.783C>T NP_000065.1:p.Leu261=
NM_000074.3:c.783C>T MANE Select NP_000065.1:p.Leu261=