Linked Data
dbSNP Id:
rs1557276140
gnomAD v2:
X-154132404-TAA-T
gnomAD v3:
X-154904129-TAA-T
gnomAD v4:
X-154904129-TAA-T
MyVariant Identifiers:
chrX:g.154132405_154132406del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154904130_154904131del , CM000685.2:g.154904130_154904131del | GRCh38 |
| NC_000023.10:g.154132405_154132406del , CM000685.1:g.154132405_154132406del | GRCh37 |
| NC_000023.9:g.153785599_153785600del | NCBI36 |
| NG_011403.1:g.123593_123594del | |
| NG_011403.2:g.123593_123594del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5816-43_5816-42del MANE Select | ENSP00000353393.4:n.5816-43_5816-42del | |
| ENST00000360256.8:c.5816-43_5816-42del | ENSP00000353393.4:n.5816-43_5816-42del | |
| NM_000132.3:c.5816-43_5816-42del | NP_000123.1:n.5816-43_5816-42del | |
| XM_011531126.1:c.5711-43_5711-42del | XP_011529428.1:n.5711-43_5711-42del | |
| NM_000132.4:c.5816-43_5816-42del MANE Select | NP_000123.1:n.5816-43_5816-42del |