Canonical Allele Identifier: CA518856007
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741430C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659271C>A , CM000685.2:g.136659271C>A GRCh38
NC_000023.10:g.135741430C>A , CM000685.1:g.135741430C>A GRCh37
NC_000023.9:g.135569096C>A NCBI36
NG_007280.1:g.16095C>A , LRG_141:g.16095C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*260C>A ENSP00000512122.1:n.*260C>A
ENST00000695725.1:c.*197C>A ENSP00000512123.1:n.*197C>A
ENST00000695726.1:n.2610C>A
ENST00000695729.1:n.3445C>A
ENST00000370629.7:c.642C>A MANE Select ENSP00000359663.2:p.Ser214=
ENST00000370628.2:c.579C>A ENSP00000359662.2:p.Ser193=
ENST00000370629.6:c.642C>A ENSP00000359663.2:p.Ser214=
NM_000074.2:c.642C>A , LRG_141t1:c.642C>A NP_000065.1:p.Ser214=
NM_000074.3:c.642C>A MANE Select NP_000065.1:p.Ser214=