Canonical Allele Identifier: CA2695236791
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659262_136659263del , CM000685.2:g.136659262_136659263del GRCh38
NC_000023.10:g.135741421_135741422del , CM000685.1:g.135741421_135741422del GRCh37
NC_000023.9:g.135569087_135569088del NCBI36
NG_007280.1:g.16086_16087del , LRG_141:g.16086_16087del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*251_*252del ENSP00000512122.1:n.*251_*252del
ENST00000695725.1:c.*188_*189del ENSP00000512123.1:n.*188_*189del
ENST00000695726.1:n.2601_2602del
ENST00000695729.1:n.3436_3437del
ENST00000370629.7:c.633_634del MANE Select ENSP00000359663.2:p.His212GlnfsTer18
ENST00000370628.2:c.570_571del ENSP00000359662.2:p.His191GlnfsTer18
ENST00000370629.6:c.633_634del ENSP00000359663.2:p.His212GlnfsTer18
NM_000074.2:c.633_634del , LRG_141t1:c.633_634del NP_000065.1:p.His212GlnfsTer18
NM_000074.3:c.633_634del MANE Select NP_000065.1:p.His212GlnfsTer18