Linked Data
dbSNP Id:
rs1282930036
gnomAD v3:
X-72667521-TATATTTC-T
gnomAD v4:
X-72667521-TATATTTC-T
MyVariant Identifiers:
chrX:g.72667522_72667528del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.72667522_72667528del , CM000685.2:g.72667522_72667528del | GRCh38 |
| NC_000023.10:g.71887372_71887378del , CM000685.1:g.71887372_71887378del | GRCh37 |
| NC_000023.9:g.71804097_71804103del | NCBI36 |
| NG_016599.1:g.51652_51658del | |
| NG_016599.2:g.51654_51660del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000373542.9:c.619-55_619-49del MANE Select | ENSP00000362643.4:n.619-55_619-49del | |
| ENST00000339490.7:c.619-55_619-49del | ENSP00000342469.3:n.619-55_619-49del | |
| ENST00000373539.3:c.619-55_619-49del | ENSP00000362640.3:n.619-55_619-49del | |
| ENST00000373542.8:c.619-55_619-49del | ENSP00000362643.4:n.619-55_619-49del | |
| ENST00000373545.7:c.619-55_619-49del | ENSP00000362646.3:n.619-55_619-49del | |
| ENST00000541944.5:c.619-55_619-49del | ENSP00000441251.1:n.619-55_619-49del | |
| NM_001122670.1:c.619-55_619-49del | NP_001116142.1:n.619-55_619-49del | |
| NM_001172436.1:c.619-55_619-49del | NP_001165907.1:n.619-55_619-49del | |
| NM_002637.3:c.619-55_619-49del | NP_002628.2:n.619-55_619-49del | |
| XM_006724661.2:c.619-55_619-49del | XP_006724724.1:n.619-55_619-49del | |
| XR_001755696.1:n.762-55_762-49del | ||
| NM_002637.4:c.619-55_619-49del MANE Select | NP_002628.2:n.619-55_619-49del | |
| NM_001122670.2:c.619-55_619-49del | NP_001116142.1:n.619-55_619-49del | |
| NM_001172436.2:c.619-55_619-49del | NP_001165907.1:n.619-55_619-49del |