Canonical Allele Identifier: CA2694817282
Gene: CD40LG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648521_136648522insACAAACA , CM000685.2:g.136648521_136648522insACAAACA GRCh38
NC_000023.10:g.135730680_135730681insACAAACA , CM000685.1:g.135730680_135730681insACAAACA GRCh37
NC_000023.9:g.135558346_135558347insACAAACA NCBI36
NG_007280.1:g.5345_5346insACAAACA , LRG_141:g.5345_5346insACAAACA

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.156+117_156+118insACAAACA ENSP00000512122.1:n.156+117_156+118insACAAACA
ENST00000695725.1:c.156+117_156+118insACAAACA ENSP00000512123.1:n.156+117_156+118insACAAACA
ENST00000695726.1:n.199+117_199+118insACAAACA
ENST00000695727.1:n.143+117_143+118insACAAACA
ENST00000695728.1:n.143+117_143+118insACAAACA
ENST00000370629.7:c.156+117_156+118insACAAACA MANE Select ENSP00000359663.2:n.156+117_156+118insACAAACA
ENST00000370628.2:c.156+117_156+118insACAAACA ENSP00000359662.2:n.156+117_156+118insACAAACA
ENST00000370629.6:c.156+117_156+118insACAAACA ENSP00000359663.2:n.156+117_156+118insACAAACA
NM_000074.2:c.156+117_156+118insACAAACA , LRG_141t1:c.156+117_156+118insACAAACA NP_000065.1:n.156+117_156+118insACAAACA
NM_000074.3:c.156+117_156+118insACAAACA MANE Select NP_000065.1:n.156+117_156+118insACAAACA