Linked Data
dbSNP Id:
rs1557150895
gnomAD v2:
X-153363101-CG-C
gnomAD v4:
X-154097644-CG-C
MyVariant Identifiers:
chrX:g.153363102del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154097646del , CM000685.2:g.154097646del | GRCh38 |
| NC_000023.10:g.153363103del , CM000685.1:g.153363103del | GRCh37 |
| NC_000023.9:g.153016297del | NCBI36 |
| NG_007107.2:g.44477del | |
| NG_007107.3:g.44459del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000303391.11:c.-140del MANE Plus Clinical | ENSP00000301948.6:n.-140del | |
| ENST00000453960.7:c.21del MANE Select | ENSP00000395535.2:p.Ala8ArgfsTer? | |
| ENST00000303391.10:c.-140del | ENSP00000301948.6:n.-140del | |
| ENST00000369957.5:c.-140del | ENSP00000358973.4:n.-140del | |
| ENST00000407218.5:c.21del | ENSP00000384865.2:p.Ala8ArgfsTer? | |
| ENST00000453960.6:c.21del | ENSP00000395535.2:p.Ala8ArgfsTer? | |
| ENST00000619732.4:c.-140del | ENSP00000480973.1:n.-140del | |
| ENST00000627864.1:n.36del | ||
| ENST00000628176.2:c.-140del | ENSP00000486978.1:n.-140del | |
| ENST00000631210.1:n.305+7136del | ||
| NM_001110792.1:c.21del | NP_001104262.1:p.Ala8ArgfsTer? | |
| NM_001316337.1:c.-587del | NP_001303266.1:n.-587del | |
| NM_004992.3:c.-140del | NP_004983.1:n.-140del | |
| XM_005274682.3:c.-531del | XP_005274739.1:n.-531del | |
| NM_001110792.2:c.21del MANE Select | NP_001104262.1:p.Ala8ArgfsTer? | |
| NM_001316337.2:c.-587del | NP_001303266.1:n.-587del | |
| NM_001369391.2:c.-882del | NP_001356320.1:n.-882del | |
| NM_001369392.2:c.-531del | NP_001356321.1:n.-531del | |
| NM_001369393.2:c.-407del | NP_001356322.1:n.-407del | |
| NM_001386137.1:c.-812del | NP_001373066.1:n.-812del | |
| NM_001386138.1:c.-700del | NP_001373067.1:n.-700del | |
| NM_001386139.1:c.-576del | NP_001373068.1:n.-576del | |
| NM_004992.4:c.-140del MANE Plus Clinical | NP_004983.1:n.-140del |