Linked Data
ClinVar Variation Id:
422694
dbSNP Id:
rs782431608
gnomAD v2:
X-135067651-CG-C
gnomAD v3:
X-135985492-CG-C
gnomAD v4:
X-135985492-CG-C
MyVariant Identifiers:
chrX:g.135067657del (hg19)
chrX:g.135067652del (hg19)
chrX:g.135985498del (hg38)
chrX:g.135985493del (hg38)
ERepo:
CA16621203/MONDO:0010278/033
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.135985498del , CM000685.2:g.135985498del | GRCh38 |
| NC_000023.10:g.135067657del , CM000685.1:g.135067657del | GRCh37 |
| NC_000023.9:g.134895323del | NCBI36 |
| NG_017160.1:g.5072del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370695.8:c.-5del | ENSP00000359729.4:n.-5del | |
| ENST00000370701.6:c.-57+21del | ENSP00000359735.1:n.-57+21del | |
| ENST00000630721.3:c.-57+21del MANE Select | ENSP00000487486.2:n.-57+21del | |
| ENST00000636092.1:c.-56-105del | ENSP00000490406.1:n.-56-105del | |
| ENST00000636347.1:c.-35-126del | ENSP00000490648.1:n.-35-126del | |
| ENST00000637195.1:c.-35-126del | ENSP00000490330.1:n.-35-126del | |
| ENST00000637234.1:c.-56-105del | ENSP00000490527.1:n.-56-105del | |
| ENST00000637581.1:c.-56-105del | ENSP00000490731.1:n.-56-105del | |
| ENST00000678163.1:c.-5del | ENSP00000502845.1:n.-5del | |
| ENST00000370695.6:c.-5del | ENSP00000359729.4:n.-5del | |
| ENST00000370698.7:c.-5del | ENSP00000359732.3:n.-5del | |
| ENST00000370701.5:c.-57+21del | ENSP00000359735.1:n.-57+21del | |
| ENST00000627534.2:c.-57+26del | ENSP00000486743.1:n.-57+26del | |
| NM_001042537.1:c.-5del | NP_001036002.1:n.-5del | |
| NM_001177651.1:c.-57+21del | NP_001171122.1:n.-57+21del | |
| NM_006359.2:c.-5del | NP_006350.1:n.-5del | |
| XM_006724726.2:c.-57+26del | XP_006724789.1:n.-57+26del | |
| XM_011531243.1:c.-57+26del | XP_011529545.1:n.-57+26del | |
| NM_001330652.1:c.-57+26del | NP_001317581.1:n.-57+26del | |
| XM_006724726.3:c.-57+26del | XP_006724789.1:n.-57+26del | |
| XM_017029223.2:c.-56-105del | XP_016884712.1:n.-56-105del | |
| XM_017029224.1:c.-56-105del | XP_016884713.1:n.-56-105del | |
| XM_017029225.1:c.-57+21del | XP_016884714.1:n.-57+21del | |
| NM_001177651.2:c.-57+21del | NP_001171122.1:n.-57+21del | |
| NM_001330652.2:c.-57+26del | NP_001317581.1:n.-57+26del | |
| NM_006359.3:c.-5del | NP_006350.1:n.-5del | |
| NM_001042537.2:c.-5del | NP_001036002.1:n.-5del | |
| NM_001379110.1:c.-57+21del MANE Select | NP_001366039.1:n.-57+21del | |
| NM_001400909.1:c.-35-126del | NP_001387838.1:n.-35-126del | |
| NM_001400910.1:c.-56-105del | NP_001387839.1:n.-56-105del | |
| NM_001400911.1:c.-56-105del | NP_001387840.1:n.-56-105del | |
| NM_001400912.1:c.-57+26del | NP_001387841.1:n.-57+26del | |
| NM_001400913.1:c.-57+21del | NP_001387842.1:n.-57+21del |