Linked Data
ClinVar Variation Id:
1102761
ClinVar RCV Id:
RCV001426204
dbSNP Id:
rs782131315
ExAC:
X:135080633 T / TG
gnomAD v2:
X-135080633-T-TG
gnomAD v4:
X-135998474-T-TG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.135998474_135998475insG , CM000685.2:g.135998474_135998475insG | GRCh38 |
| NC_000023.10:g.135080633_135080634insG , CM000685.1:g.135080633_135080634insG | GRCh37 |
| NC_000023.9:g.134908299_134908300insG | NCBI36 |
| NG_017160.1:g.18048_18049insG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370695.8:c.604-8_604-7insG | ENSP00000359729.4:n.604-8_604-7insG | |
| ENST00000370701.6:c.448-8_448-7insG | ENSP00000359735.1:n.448-8_448-7insG | |
| ENST00000630721.3:c.448-8_448-7insG MANE Select | ENSP00000487486.2:n.448-8_448-7insG | |
| ENST00000636092.1:c.448-8_448-7insG | ENSP00000490406.1:n.448-8_448-7insG | |
| ENST00000636347.1:c.448-8_448-7insG | ENSP00000490648.1:n.448-8_448-7insG | |
| ENST00000637195.1:c.352-8_352-7insG | ENSP00000490330.1:n.352-8_352-7insG | |
| ENST00000637234.1:c.448-8_448-7insG | ENSP00000490527.1:n.448-8_448-7insG | |
| ENST00000637581.1:c.448-8_448-7insG | ENSP00000490731.1:n.448-8_448-7insG | |
| ENST00000643775.1:n.391-8_391-7insG | ||
| ENST00000674809.1:c.391-8_391-7insG | ENSP00000502455.1:n.391-8_391-7insG | |
| ENST00000675550.1:n.389-8_389-7insG | ||
| ENST00000675856.1:n.391-8_391-7insG | ||
| ENST00000676043.1:c.391-8_391-7insG | ENSP00000501920.1:n.391-8_391-7insG | |
| ENST00000678163.1:c.604-8_604-7insG | ENSP00000502845.1:n.604-8_604-7insG | |
| ENST00000370695.6:c.604-8_604-7insG | ENSP00000359729.4:n.604-8_604-7insG | |
| ENST00000370698.7:c.508-8_508-7insG | ENSP00000359732.3:n.508-8_508-7insG | |
| ENST00000370701.5:c.448-8_448-7insG | ENSP00000359735.1:n.448-8_448-7insG | |
| ENST00000627534.2:c.448-8_448-7insG | ENSP00000486743.1:n.448-8_448-7insG | |
| NM_001042537.1:c.604-8_604-7insG | NP_001036002.1:n.604-8_604-7insG | |
| NM_001177651.1:c.448-8_448-7insG | NP_001171122.1:n.448-8_448-7insG | |
| NM_006359.2:c.508-8_508-7insG | NP_006350.1:n.508-8_508-7insG | |
| XM_006724726.2:c.448-8_448-7insG | XP_006724789.1:n.448-8_448-7insG | |
| XM_011531243.1:c.352-8_352-7insG | XP_011529545.1:n.352-8_352-7insG | |
| NM_001330652.1:c.352-8_352-7insG | NP_001317581.1:n.352-8_352-7insG | |
| XM_006724726.3:c.448-8_448-7insG | XP_006724789.1:n.448-8_448-7insG | |
| XM_017029223.2:c.448-8_448-7insG | XP_016884712.1:n.448-8_448-7insG | |
| XM_017029224.1:c.448-8_448-7insG | XP_016884713.1:n.448-8_448-7insG | |
| XM_017029225.1:c.352-8_352-7insG | XP_016884714.1:n.352-8_352-7insG | |
| NM_001177651.2:c.448-8_448-7insG | NP_001171122.1:n.448-8_448-7insG | |
| NM_001330652.2:c.352-8_352-7insG | NP_001317581.1:n.352-8_352-7insG | |
| NM_006359.3:c.508-8_508-7insG | NP_006350.1:n.508-8_508-7insG | |
| NM_001042537.2:c.604-8_604-7insG | NP_001036002.1:n.604-8_604-7insG | |
| NM_001379110.1:c.448-8_448-7insG MANE Select | NP_001366039.1:n.448-8_448-7insG | |
| NM_001400909.1:c.448-8_448-7insG | NP_001387838.1:n.448-8_448-7insG | |
| NM_001400910.1:c.448-8_448-7insG | NP_001387839.1:n.448-8_448-7insG | |
| NM_001400911.1:c.448-8_448-7insG | NP_001387840.1:n.448-8_448-7insG | |
| NM_001400912.1:c.448-8_448-7insG | NP_001387841.1:n.448-8_448-7insG | |
| NM_001400913.1:c.352-8_352-7insG | NP_001387842.1:n.352-8_352-7insG |