Canonical Allele Identifier: CA518856024
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741457T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659298T>A , CM000685.2:g.136659298T>A GRCh38
NC_000023.10:g.135741457T>A , CM000685.1:g.135741457T>A GRCh37
NC_000023.9:g.135569123T>A NCBI36
NG_007280.1:g.16122T>A , LRG_141:g.16122T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*287T>A ENSP00000512122.1:n.*287T>A
ENST00000695725.1:c.*224T>A ENSP00000512123.1:n.*224T>A
ENST00000695726.1:n.2637T>A
ENST00000695729.1:n.3472T>A
ENST00000370629.7:c.669T>A MANE Select ENSP00000359663.2:p.Ile223=
ENST00000370628.2:c.606T>A ENSP00000359662.2:p.Ile202=
ENST00000370629.6:c.669T>A ENSP00000359663.2:p.Ile223=
NM_000074.2:c.669T>A , LRG_141t1:c.669T>A NP_000065.1:p.Ile223=
NM_000074.3:c.669T>A MANE Select NP_000065.1:p.Ile223=
Search 100 bp 5'
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