Linked Data
dbSNP Id:
rs1419842051
gnomAD v4:
X-153740326-GTCAGCACC-G
MyVariant Identifiers:
chrX:g.153740327_153740334del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153740331_153740338del , CM000685.2:g.153740331_153740338del | GRCh38 |
| NC_000023.10:g.153005785_153005792del , CM000685.1:g.153005785_153005792del | GRCh37 |
| NC_000023.9:g.152658979_152658986del | NCBI36 |
| NG_009022.2:g.20464_20471del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000218104.6:c.1634+94_1634+101del MANE Select | ENSP00000218104.3:n.1634+94_1634+101del | |
| ENST00000218104.5:c.1634+94_1634+101del | ENSP00000218104.3:n.1634+94_1634+101del | |
| ENST00000443684.2:n.637+94_637+101del | ||
| NM_000033.3:c.1634+94_1634+101del | NP_000024.2:n.1634+94_1634+101del | |
| XR_938507.1:n.2106+94_2106+101del | ||
| XR_938507.2:n.2106+94_2106+101del | ||
| NM_000033.4:c.1634+94_1634+101del MANE Select | NP_000024.2:n.1634+94_1634+101del |