Canonical Allele Identifier: CA518856011
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741433C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659274C>A , CM000685.2:g.136659274C>A GRCh38
NC_000023.10:g.135741433C>A , CM000685.1:g.135741433C>A GRCh37
NC_000023.9:g.135569099C>A NCBI36
NG_007280.1:g.16098C>A , LRG_141:g.16098C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*263C>A ENSP00000512122.1:n.*263C>A
ENST00000695725.1:c.*200C>A ENSP00000512123.1:n.*200C>A
ENST00000695726.1:n.2613C>A
ENST00000695729.1:n.3448C>A
ENST00000370629.7:c.645C>A MANE Select ENSP00000359663.2:p.Ala215=
ENST00000370628.2:c.582C>A ENSP00000359662.2:p.Ala194=
ENST00000370629.6:c.645C>A ENSP00000359663.2:p.Ala215=
NM_000074.2:c.645C>A , LRG_141t1:c.645C>A NP_000065.1:p.Ala215=
NM_000074.3:c.645C>A MANE Select NP_000065.1:p.Ala215=