Canonical Allele Identifier: CA871926203

Gene: CD40LG

Linked Data

• dbSNP Id: rs1231955531
• gnomAD v3: X-136648530-GTTGCC-G
• gnomAD v4: X-136648530-GTTGCC-G
• MyVariant Identifiers: chrX:g.135730690_135730694del (hg19) ; chrX:g.136648531_136648535del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136648532_136648536del , CM000685.2:g.136648532_136648536del	GRCh38
NC_000023.10:g.135730691_135730695del , CM000685.1:g.135730691_135730695del	GRCh37
NC_000023.9:g.135558357_135558361del	NCBI36
NG_007280.1:g.5356_5360del , LRG_141:g.5356_5360del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.156+128_156+132del	ENSP00000512122.1:n.156+128_156+132del
ENST00000695725.1:c.156+128_156+132del	ENSP00000512123.1:n.156+128_156+132del
ENST00000695726.1:n.199+128_199+132del
ENST00000695727.1:n.143+128_143+132del
ENST00000695728.1:n.143+128_143+132del
ENST00000370629.7:c.156+128_156+132del MANE Select	ENSP00000359663.2:n.156+128_156+132del
ENST00000370628.2:c.156+128_156+132del	ENSP00000359662.2:n.156+128_156+132del
ENST00000370629.6:c.156+128_156+132del	ENSP00000359663.2:n.156+128_156+132del
NM_000074.2:c.156+128_156+132del , LRG_141t1:c.156+128_156+132del	NP_000065.1:n.156+128_156+132del
NM_000074.3:c.156+128_156+132del MANE Select	NP_000065.1:n.156+128_156+132del