Canonical Allele Identifier: CA414752235
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648404G>C , CM000685.2:g.136648404G>C GRCh38
NC_000023.10:g.135730563G>C , CM000685.1:g.135730563G>C GRCh37
NC_000023.9:g.135558229G>C NCBI36
NG_007280.1:g.5228G>C , LRG_141:g.5228G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.156G>C ENSP00000512122.1:p.Lys52Asn
ENST00000695725.1:c.156G>C ENSP00000512123.1:p.Lys52Asn
ENST00000695726.1:n.199G>C
ENST00000695727.1:n.143G>C
ENST00000695728.1:n.143G>C
ENST00000370629.7:c.156G>C MANE Select ENSP00000359663.2:p.Lys52Asn
ENST00000370628.2:c.156G>C ENSP00000359662.2:p.Lys52Asn
ENST00000370629.6:c.156G>C ENSP00000359663.2:p.Lys52Asn
NM_000074.2:c.156G>C , LRG_141t1:c.156G>C NP_000065.1:p.Lys52Asn
NM_000074.3:c.156G>C MANE Select NP_000065.1:p.Lys52Asn