Canonical Allele Identifier: CA1137626169
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs2076094516
gnomAD v3: X-136648180-TTGAC-T
gnomAD v4: X-136648180-TTGAC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136648181_136648184del , CM000685.2:g.136648181_136648184del GRCh38
NC_000023.10:g.135730340_135730343del , CM000685.1:g.135730340_135730343del GRCh37
NC_000023.9:g.135558006_135558009del NCBI36
NG_007280.1:g.5005_5008del , LRG_141:g.5005_5008del

Transcript Alleles

HGVS Amino-acid change
ENST00000695724.1:c.-68_-65del ENSP00000512122.1:n.-68_-65del
ENST00000695725.1:c.-68_-65del ENSP00000512123.1:n.-68_-65del
ENST00000370629.7:c.-68_-65del MANE Select ENSP00000359663.2:n.-68_-65del
NM_000074.2:c.-68_-65del , LRG_141t1:c.-68_-65del NP_000065.1:n.-68_-65del
NM_000074.3:c.-68_-65del MANE Select NP_000065.1:n.-68_-65del
Search 100 bp 5'
Search 100 bp 3'