Linked Data
dbSNP Id:
rs1555976462
gnomAD v2:
X-100603703-T-TTCATGTATTTACTGGGAGG
MyVariant Identifiers:
chrX:g.100603703_100603704insTCATGTATTTACTGGGAGG (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101348715_101348716insTCATGTATTTACTGGGAGG , CM000685.2:g.101348715_101348716insTCATGTATTTACTGGGAGG | GRCh38 |
| NC_000023.10:g.100603703_100603704insTCATGTATTTACTGGGAGG , CM000685.1:g.100603703_100603704insTCATGTATTTACTGGGAGG | GRCh37 |
| NC_000023.9:g.100490359_100490360insTCATGTATTTACTGGGAGG | NCBI36 |
| NG_009616.1:g.42509_42510insCCTCCCAGTAAATACATGA , LRG_128:g.42509_42510insCCTCCCAGTAAATACATGA | |
| NG_011734.1:g.5254_5255insCCTCCCAGTAAATACATGA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372902.4:c.-52_-51insCCTCCCAGTAAATACATGA MANE Select | ENSP00000361993.3:n.-52_-51insCCTCCCAGTAAATACATGA | |
| ENST00000644112.2:c.-52_-51insCCTCCCAGTAAATACATGA | ENSP00000494385.1:n.-52_-51insCCTCCCAGTAAATACATGA | |
| ENST00000372902.3:c.-52_-51insCCTCCCAGTAAATACATGA | ENSP00000361993.3:n.-52_-51insCCTCCCAGTAAATACATGA | |
| ENST00000480575.1:n.34_35insCCTCCCAGTAAATACATGA | ||
| NM_001145951.1:c.-52_-51insCCTCCCAGTAAATACATGA | NP_001139423.1:n.-52_-51insCCTCCCAGTAAATACATGA | |
| NM_004085.3:c.-52_-51insCCTCCCAGTAAATACATGA | NP_004076.1:n.-52_-51insCCTCCCAGTAAATACATGA | |
| NM_004085.4:c.-52_-51insCCTCCCAGTAAATACATGA MANE Select | NP_004076.1:n.-52_-51insCCTCCCAGTAAATACATGA | |
| NM_001145951.2:c.-52_-51insCCTCCCAGTAAATACATGA | NP_001139423.1:n.-52_-51insCCTCCCAGTAAATACATGA |