Canonical Allele Identifier: CA2695236781
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659175_136659176insATA , CM000685.2:g.136659175_136659176insATA GRCh38
NC_000023.10:g.135741334_135741335insATA , CM000685.1:g.135741334_135741335insATA GRCh37
NC_000023.9:g.135569000_135569001insATA NCBI36
NG_007280.1:g.15999_16000insATA , LRG_141:g.15999_16000insATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*164_*165insATA ENSP00000512122.1:n.*164_*165insATA
ENST00000695725.1:c.*101_*102insATA ENSP00000512123.1:n.*101_*102insATA
ENST00000695726.1:n.2514_2515insATA
ENST00000695729.1:n.3349_3350insATA
ENST00000370629.7:c.546_547insATA MANE Select ENSP00000359663.2:p.Glu182_Ala183insIle
ENST00000370628.2:c.483_484insATA ENSP00000359662.2:p.Glu161_Ala162insIle
ENST00000370629.6:c.546_547insATA ENSP00000359663.2:p.Glu182_Ala183insIle
NM_000074.2:c.546_547insATA , LRG_141t1:c.546_547insATA NP_000065.1:p.Glu182_Ala183insIle
NM_000074.3:c.546_547insATA MANE Select NP_000065.1:p.Glu182_Ala183insIle