Canonical Allele Identifier: CA518855824
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741223C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659064C>T , CM000685.2:g.136659064C>T GRCh38
NC_000023.10:g.135741223C>T , CM000685.1:g.135741223C>T GRCh37
NC_000023.9:g.135568889C>T NCBI36
NG_007280.1:g.15888C>T , LRG_141:g.15888C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*53C>T ENSP00000512122.1:n.*53C>T
ENST00000695725.1:c.182C>T ENSP00000512123.1:p.Thr61Ile
ENST00000695726.1:n.2403C>T
ENST00000695729.1:n.3238C>T
ENST00000370629.7:c.435C>T MANE Select ENSP00000359663.2:p.Tyr145=
ENST00000370628.2:c.372C>T ENSP00000359662.2:p.Tyr124=
ENST00000370629.6:c.435C>T ENSP00000359663.2:p.Tyr145=
NM_000074.2:c.435C>T , LRG_141t1:c.435C>T NP_000065.1:p.Tyr145=
NM_000074.3:c.435C>T MANE Select NP_000065.1:p.Tyr145=