Canonical Allele Identifier: CA414756913
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659366A>G , CM000685.2:g.136659366A>G GRCh38
NC_000023.10:g.135741525A>G , CM000685.1:g.135741525A>G GRCh37
NC_000023.9:g.135569191A>G NCBI36
NG_007280.1:g.16190A>G , LRG_141:g.16190A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*355A>G ENSP00000512122.1:n.*355A>G
ENST00000695725.1:c.*292A>G ENSP00000512123.1:n.*292A>G
ENST00000695726.1:n.2705A>G
ENST00000695729.1:n.3540A>G
ENST00000370629.7:c.737A>G MANE Select ENSP00000359663.2:p.Gln246Arg
ENST00000370628.2:c.674A>G ENSP00000359662.2:p.Gln225Arg
ENST00000370629.6:c.737A>G ENSP00000359663.2:p.Gln246Arg
NM_000074.2:c.737A>G , LRG_141t1:c.737A>G NP_000065.1:p.Gln246Arg
NM_000074.3:c.737A>G MANE Select NP_000065.1:p.Gln246Arg