Canonical Allele Identifier: CA414756250
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659264A>G , CM000685.2:g.136659264A>G GRCh38
NC_000023.10:g.135741423A>G , CM000685.1:g.135741423A>G GRCh37
NC_000023.9:g.135569089A>G NCBI36
NG_007280.1:g.16088A>G , LRG_141:g.16088A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*253A>G ENSP00000512122.1:n.*253A>G
ENST00000695725.1:c.*190A>G ENSP00000512123.1:n.*190A>G
ENST00000695726.1:n.2603A>G
ENST00000695729.1:n.3438A>G
ENST00000370629.7:c.635A>G MANE Select ENSP00000359663.2:p.His212Arg
ENST00000370628.2:c.572A>G ENSP00000359662.2:p.His191Arg
ENST00000370629.6:c.635A>G ENSP00000359663.2:p.His212Arg
NM_000074.2:c.635A>G , LRG_141t1:c.635A>G NP_000065.1:p.His212Arg
NM_000074.3:c.635A>G MANE Select NP_000065.1:p.His212Arg