Canonical Allele Identifier: CA518856036
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741475T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659316T>C , CM000685.2:g.136659316T>C GRCh38
NC_000023.10:g.135741475T>C , CM000685.1:g.135741475T>C GRCh37
NC_000023.9:g.135569141T>C NCBI36
NG_007280.1:g.16140T>C , LRG_141:g.16140T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*305T>C ENSP00000512122.1:n.*305T>C
ENST00000695725.1:c.*242T>C ENSP00000512123.1:n.*242T>C
ENST00000695726.1:n.2655T>C
ENST00000695729.1:n.3490T>C
ENST00000370629.7:c.687T>C MANE Select ENSP00000359663.2:p.Phe229=
ENST00000370628.2:c.624T>C ENSP00000359662.2:p.Phe208=
ENST00000370629.6:c.687T>C ENSP00000359663.2:p.Phe229=
NM_000074.2:c.687T>C , LRG_141t1:c.687T>C NP_000065.1:p.Phe229=
NM_000074.3:c.687T>C MANE Select NP_000065.1:p.Phe229=