Canonical Allele Identifier: CA2695236792
Gene: CD40LG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659265_136659266del , CM000685.2:g.136659265_136659266del GRCh38
NC_000023.10:g.135741424_135741425del , CM000685.1:g.135741424_135741425del GRCh37
NC_000023.9:g.135569090_135569091del NCBI36
NG_007280.1:g.16089_16090del , LRG_141:g.16089_16090del

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*254_*255del ENSP00000512122.1:n.*254_*255del
ENST00000695725.1:c.*191_*192del ENSP00000512123.1:n.*191_*192del
ENST00000695726.1:n.2604_2605del
ENST00000695729.1:n.3439_3440del
ENST00000370629.7:c.636_637del MANE Select ENSP00000359663.2:p.His212GlnfsTer18
ENST00000370628.2:c.573_574del ENSP00000359662.2:p.His191GlnfsTer18
ENST00000370629.6:c.636_637del ENSP00000359663.2:p.His212GlnfsTer18
NM_000074.2:c.636_637del , LRG_141t1:c.636_637del NP_000065.1:p.His212GlnfsTer18
NM_000074.3:c.636_637del MANE Select NP_000065.1:p.His212GlnfsTer18