Canonical Allele Identifier: CA2695236777
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659150_136659151del , CM000685.2:g.136659150_136659151del GRCh38
NC_000023.10:g.135741309_135741310del , CM000685.1:g.135741309_135741310del GRCh37
NC_000023.9:g.135568975_135568976del NCBI36
NG_007280.1:g.15974_15975del , LRG_141:g.15974_15975del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*139_*140del ENSP00000512122.1:n.*139_*140del
ENST00000695725.1:c.*76_*77del ENSP00000512123.1:n.*76_*77del
ENST00000695726.1:n.2489_2490del
ENST00000695729.1:n.3324_3325del
ENST00000370629.7:c.521_522del MANE Select ENSP00000359663.2:p.Gln174ArgfsTer26
ENST00000370628.2:c.458_459del ENSP00000359662.2:p.Gln153ArgfsTer26
ENST00000370629.6:c.521_522del ENSP00000359663.2:p.Gln174ArgfsTer26
NM_000074.2:c.521_522del , LRG_141t1:c.521_522del NP_000065.1:p.Gln174ArgfsTer26
NM_000074.3:c.521_522del MANE Select NP_000065.1:p.Gln174ArgfsTer26