Canonical Allele Identifier: CA518855930
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741313C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659154C>G , CM000685.2:g.136659154C>G GRCh38
NC_000023.10:g.135741313C>G , CM000685.1:g.135741313C>G GRCh37
NC_000023.9:g.135568979C>G NCBI36
NG_007280.1:g.15978C>G , LRG_141:g.15978C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*143C>G ENSP00000512122.1:n.*143C>G
ENST00000695725.1:c.*80C>G ENSP00000512123.1:n.*80C>G
ENST00000695726.1:n.2493C>G
ENST00000695729.1:n.3328C>G
ENST00000370629.7:c.525C>G MANE Select ENSP00000359663.2:p.Val175=
ENST00000370628.2:c.462C>G ENSP00000359662.2:p.Val154=
ENST00000370629.6:c.525C>G ENSP00000359663.2:p.Val175=
NM_000074.2:c.525C>G , LRG_141t1:c.525C>G NP_000065.1:p.Val175=
NM_000074.3:c.525C>G MANE Select NP_000065.1:p.Val175=