Linked Data
dbSNP Id:
rs1557061207
gnomAD v2:
X-153035771-TG-T
gnomAD v4:
X-153770316-TG-T
MyVariant Identifiers:
chrX:g.153035772del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153770317del , CM000685.2:g.153770317del | GRCh38 |
| NC_000023.10:g.153035772del , CM000685.1:g.153035772del | GRCh37 |
| NC_000023.9:g.152688966del | NCBI36 |
| NG_013255.1:g.11122del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361971.10:c.1787-21del MANE Select | ENSP00000355378.5:n.1787-21del | |
| ENST00000361971.9:c.1787-21del | ENSP00000355378.5:n.1787-21del | |
| ENST00000538966.5:c.1856-21del | ENSP00000442736.1:n.1856-21del | |
| NM_001163257.1:c.1856-21del | NP_001156729.1:n.1856-21del | |
| NM_005393.2:c.1787-21del | NP_005384.2:n.1787-21del | |
| NM_005393.3:c.1787-21del MANE Select | NP_005384.2:n.1787-21del | |
| NM_001163257.2:c.1856-21del | NP_001156729.1:n.1856-21del |