Canonical Allele Identifier: CA414751567
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648294G>A , CM000685.2:g.136648294G>A GRCh38
NC_000023.10:g.135730453G>A , CM000685.1:g.135730453G>A GRCh37
NC_000023.9:g.135558119G>A NCBI36
NG_007280.1:g.5118G>A , LRG_141:g.5118G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.46G>A ENSP00000512122.1:p.Gly16Arg
ENST00000695725.1:c.46G>A ENSP00000512123.1:p.Gly16Arg
ENST00000695726.1:n.89G>A
ENST00000695727.1:n.33G>A
ENST00000695728.1:n.33G>A
ENST00000370629.7:c.46G>A MANE Select ENSP00000359663.2:p.Gly16Arg
ENST00000370628.2:c.46G>A ENSP00000359662.2:p.Gly16Arg
ENST00000370629.6:c.46G>A ENSP00000359663.2:p.Gly16Arg
NM_000074.2:c.46G>A , LRG_141t1:c.46G>A NP_000065.1:p.Gly16Arg
NM_000074.3:c.46G>A MANE Select NP_000065.1:p.Gly16Arg