Canonical Allele Identifier: CA644630472

Gene: CD40LG

Linked Data

• dbSNP Id: rs1569375836
• gnomAD v2: X-135730574-C-CTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA
• gnomAD v3: X-136648415-C-CTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA
• gnomAD v4: X-136648415-C-CTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA
• MyVariant Identifiers: chrX:g.135730574_135730575insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648415_136648416insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA , CM000685.2:g.136648415_136648416insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA	GRCh38
NC_000023.10:g.135730574_135730575insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA , CM000685.1:g.135730574_135730575insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA	GRCh37
NC_000023.9:g.135558240_135558241insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA	NCBI36
NG_007280.1:g.5239_5240insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA , LRG_141:g.5239_5240insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.156+11_156+12insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA	ENSP00000512122.1:n.156+11_156+12insTTCATGAAGATTTTGTATTCATGAA...
ENST00000695725.1:c.156+11_156+12insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA	ENSP00000512123.1:n.156+11_156+12insTTCATGAAGATTTTGTATTCATGAA...
ENST00000695726.1:n.199+11_199+12insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA
ENST00000695727.1:n.143+11_143+12insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA
ENST00000695728.1:n.143+11_143+12insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA
ENST00000370629.7:c.156+11_156+12insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA MANE Select	ENSP00000359663.2:n.156+11_156+12insTTCATGAAGATTTTGTATTCATGAA...
ENST00000370628.2:c.156+11_156+12insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA	ENSP00000359662.2:n.156+11_156+12insTTCATGAAGATTTTGTATTCATGAA...
ENST00000370629.6:c.156+11_156+12insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA	ENSP00000359663.2:n.156+11_156+12insTTCATGAAGATTTTGTATTCATGAA...
NM_000074.2:c.156+11_156+12insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA , LRG_141t1:c.156+11_156+12insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA	NP_000065.1:n.156+11_156+12insTTCATGAAGATTTTGTATTCATGAAAACGAT...
NM_000074.3:c.156+11_156+12insTTCATGAAGATTTTGTATTCATGAAAACGATACAGAGATGCAA MANE Select	NP_000065.1:n.156+11_156+12insTTCATGAAGATTTTGTATTCATGAAAACGAT...