Canonical Allele Identifier: CA2695236802
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659365_136659369del , CM000685.2:g.136659365_136659369del GRCh38
NC_000023.10:g.135741524_135741528del , CM000685.1:g.135741524_135741528del GRCh37
NC_000023.9:g.135569190_135569194del NCBI36
NG_007280.1:g.16189_16193del , LRG_141:g.16189_16193del

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.*354_*358del ENSP00000512122.1:n.*354_*358del
ENST00000695725.1:c.*291_*295del ENSP00000512123.1:n.*291_*295del
ENST00000695726.1:n.2704_2708del
ENST00000695729.1:n.3539_3543del
ENST00000370629.7:c.736_740del MANE Select ENSP00000359663.2:p.Gln246GlufsTer?
ENST00000370628.2:c.673_677del ENSP00000359662.2:p.Gln225GlufsTer?
ENST00000370629.6:c.736_740del ENSP00000359663.2:p.Gln246GlufsTer?
NM_000074.2:c.736_740del , LRG_141t1:c.736_740del NP_000065.1:p.Gln246GlufsTer?
NM_000074.3:c.736_740del MANE Select NP_000065.1:p.Gln246GlufsTer?