Canonical Allele Identifier: CA644630701

Gene: CD40LG

Linked Data

• dbSNP Id: rs747178822
• gnomAD v2: X-135741574-A-ACTCG
• gnomAD v3: X-136659415-A-ACTCG
• gnomAD v4: X-136659415-A-ACTCG
• MyVariant Identifiers: chrX:g.135741574_135741575insCTCG (hg19) ; chrX:g.136659415_136659416insCTCG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659415_136659416insCTCG , CM000685.2:g.136659415_136659416insCTCG	GRCh38
NC_000023.10:g.135741574_135741575insCTCG , CM000685.1:g.135741574_135741575insCTCG	GRCh37
NC_000023.9:g.135569240_135569241insCTCG	NCBI36
NG_007280.1:g.16239_16240insCTCG , LRG_141:g.16239_16240insCTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*404_*405insCTCG	ENSP00000512122.1:n.*404_*405insCTCG
ENST00000695725.1:c.*341_*342insCTCG	ENSP00000512123.1:n.*341_*342insCTCG
ENST00000695726.1:n.2754_2755insCTCG
ENST00000695729.1:n.3589_3590insCTCG
ENST00000370629.7:c.786_*1insCTCG MANE Select	ENSP00000359663.2:n.786_*1insCTCG
ENST00000370628.2:c.723_*1insCTCG	ENSP00000359662.2:n.723_*1insCTCG
ENST00000370629.6:c.786_*1insCTCG	ENSP00000359663.2:n.786_*1insCTCG
NM_000074.2:c.786_*1insCTCG , LRG_141t1:c.786_*1insCTCG	NP_000065.1:n.786_*1insCTCG
NM_000074.3:c.786_*1insCTCG MANE Select	NP_000065.1:n.786_*1insCTCG