Canonical Allele Identifier: CA644630702

Gene: CD40LG

Linked Data

• dbSNP Id: rs1356063965
• gnomAD v2: X-135741575-A-AGGGATCCAGATCTGCTGTGCCTTCTAGTTGC
• MyVariant Identifiers: chrX:g.135741575_135741576insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC (hg19) ; chrX:g.136659416_136659417insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136659416_136659417insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC , CM000685.2:g.136659416_136659417insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC	GRCh38
NC_000023.10:g.135741575_135741576insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC , CM000685.1:g.135741575_135741576insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC	GRCh37
NC_000023.9:g.135569241_135569242insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC	NCBI36
NG_007280.1:g.16240_16241insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC , LRG_141:g.16240_16241insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695724.1:c.*405_*406insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC	ENSP00000512122.1:n.*405_*406insGGGATCCAGATCTGCTGTGCCTTCTAGTT...
ENST00000695725.1:c.*342_*343insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC	ENSP00000512123.1:n.*342_*343insGGGATCCAGATCTGCTGTGCCTTCTAGTT...
ENST00000695726.1:n.2755_2756insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC
ENST00000695729.1:n.3590_3591insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC
ENST00000370629.7:c.*1_*2insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC MANE Select	ENSP00000359663.2:n.*1_*2insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC
ENST00000370628.2:c.*1_*2insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC	ENSP00000359662.2:n.*1_*2insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC
ENST00000370629.6:c.*1_*2insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC	ENSP00000359663.2:n.*1_*2insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC
NM_000074.2:c.*1_*2insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC , LRG_141t1:c.*1_*2insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC	NP_000065.1:n.*1_*2insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC
NM_000074.3:c.*1_*2insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC MANE Select	NP_000065.1:n.*1_*2insGGGATCCAGATCTGCTGTGCCTTCTAGTTGC