Canonical Allele Identifier: CA518856034
Gene: CD40LG HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.135741472A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659313A>C , CM000685.2:g.136659313A>C GRCh38
NC_000023.10:g.135741472A>C , CM000685.1:g.135741472A>C GRCh37
NC_000023.9:g.135569138A>C NCBI36
NG_007280.1:g.16137A>C , LRG_141:g.16137A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*302A>C ENSP00000512122.1:n.*302A>C
ENST00000695725.1:c.*239A>C ENSP00000512123.1:n.*239A>C
ENST00000695726.1:n.2652A>C
ENST00000695729.1:n.3487A>C
ENST00000370629.7:c.684A>C MANE Select ENSP00000359663.2:p.Val228=
ENST00000370628.2:c.621A>C ENSP00000359662.2:p.Val207=
ENST00000370629.6:c.684A>C ENSP00000359663.2:p.Val228=
NM_000074.2:c.684A>C , LRG_141t1:c.684A>C NP_000065.1:p.Val228=
NM_000074.3:c.684A>C MANE Select NP_000065.1:p.Val228=