Canonical Allele Identifier: CA414756289
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659268T>G , CM000685.2:g.136659268T>G GRCh38
NC_000023.10:g.135741427T>G , CM000685.1:g.135741427T>G GRCh37
NC_000023.9:g.135569093T>G NCBI36
NG_007280.1:g.16092T>G , LRG_141:g.16092T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*257T>G ENSP00000512122.1:n.*257T>G
ENST00000695725.1:c.*194T>G ENSP00000512123.1:n.*194T>G
ENST00000695726.1:n.2607T>G
ENST00000695729.1:n.3442T>G
ENST00000370629.7:c.639T>G MANE Select ENSP00000359663.2:p.Ser213Arg
ENST00000370628.2:c.576T>G ENSP00000359662.2:p.Ser192Arg
ENST00000370629.6:c.639T>G ENSP00000359663.2:p.Ser213Arg
NM_000074.2:c.639T>G , LRG_141t1:c.639T>G NP_000065.1:p.Ser213Arg
NM_000074.3:c.639T>G MANE Select NP_000065.1:p.Ser213Arg