Canonical Allele Identifier: CA10528177
Gene: CD40LG HGNC NCBI

Linked Data

dbSNP Id: rs747178822

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136659415_136659416insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC , CM000685.2:g.136659415_136659416insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC GRCh38
NC_000023.10:g.135741574_135741575insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC , CM000685.1:g.135741574_135741575insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC GRCh37
NC_000023.9:g.135569240_135569241insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC NCBI36
NG_007280.1:g.16239_16240insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC , LRG_141:g.16239_16240insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695724.1:c.*404_*405insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC ENSP00000512122.1:n.*404_*405insCTCGAGGGATCCAGATCTGCTGTGCCTTC...
ENST00000695725.1:c.*341_*342insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC ENSP00000512123.1:n.*341_*342insCTCGAGGGATCCAGATCTGCTGTGCCTTC...
ENST00000695726.1:n.2754_2755insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC
ENST00000695729.1:n.3589_3590insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC
ENST00000370629.7:c.786_*1insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC MANE Select ENSP00000359663.2:n.786_*1insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAG...
ENST00000370628.2:c.723_*1insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC ENSP00000359662.2:n.723_*1insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAG...
ENST00000370629.6:c.786_*1insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC ENSP00000359663.2:n.786_*1insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAG...
NM_000074.2:c.786_*1insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC , LRG_141t1:c.786_*1insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC NP_000065.1:n.786_*1insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCA...
NM_000074.3:c.786_*1insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCAGCC MANE Select NP_000065.1:n.786_*1insCTCGAGGGATCCAGATCTGCTGTGCCTTCTAGTTGCCA...