Canonical Allele Identifier: CA336266062

Gene: CD40LG

Linked Data

• dbSNP Id: rs76208033

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648521_136648522insAA , CM000685.2:g.136648521_136648522insAA	GRCh38
NC_000023.10:g.135730680_135730681insAA , CM000685.1:g.135730680_135730681insAA	GRCh37
NC_000023.9:g.135558346_135558347insAA	NCBI36
NG_007280.1:g.5345_5346insAA , LRG_141:g.5345_5346insAA

Transcript Alleles

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