Canonical Allele Identifier: CA518856072
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs2076128053
MyVariant Identifiers: chrX:g.135741532C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659373C>T , CM000685.2:g.136659373C>T GRCh38
NC_000023.10:g.135741532C>T , CM000685.1:g.135741532C>T GRCh37
NC_000023.9:g.135569198C>T NCBI36
NG_007280.1:g.16197C>T , LRG_141:g.16197C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*362C>T ENSP00000512122.1:n.*362C>T
ENST00000695725.1:c.*299C>T ENSP00000512123.1:n.*299C>T
ENST00000695726.1:n.2712C>T
ENST00000695729.1:n.3547C>T
ENST00000370629.7:c.744C>T MANE Select ENSP00000359663.2:p.Ser248=
ENST00000370628.2:c.681C>T ENSP00000359662.2:p.Ser227=
ENST00000370629.6:c.744C>T ENSP00000359663.2:p.Ser248=
NM_000074.2:c.744C>T , LRG_141t1:c.744C>T NP_000065.1:p.Ser248=
NM_000074.3:c.744C>T MANE Select NP_000065.1:p.Ser248=