Linked Data
ClinVar Variation Id:
1570721
ClinVar RCV Id:
RCV002215587
dbSNP Id:
rs1292220528
gnomAD v4:
X-135998505-G-T
MyVariant Identifiers:
chrX:g.135080664G>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.135998505G>T , CM000685.2:g.135998505G>T | GRCh38 |
| NC_000023.10:g.135080664G>T , CM000685.1:g.135080664G>T | GRCh37 |
| NC_000023.9:g.134908330G>T | NCBI36 |
| NG_017160.1:g.18079G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000370695.8:c.627G>T | ENSP00000359729.4:p.Gly209= | |
| ENST00000370701.6:c.471G>T | ENSP00000359735.1:p.Gly157= | |
| ENST00000630721.3:c.471G>T MANE Select | ENSP00000487486.2:p.Gly157= | |
| ENST00000636092.1:c.471G>T | ENSP00000490406.1:p.Gly157= | |
| ENST00000636347.1:c.471G>T | ENSP00000490648.1:p.Gly157= | |
| ENST00000637195.1:c.375G>T | ENSP00000490330.1:p.Gly125= | |
| ENST00000637234.1:c.471G>T | ENSP00000490527.1:p.Gly157= | |
| ENST00000637581.1:c.471G>T | ENSP00000490731.1:p.Gly157= | |
| ENST00000643775.1:n.414G>T | ||
| ENST00000674809.1:c.414G>T | ENSP00000502455.1:p.Gly138= | |
| ENST00000675550.1:n.412G>T | ||
| ENST00000675856.1:n.414G>T | ||
| ENST00000676043.1:c.414G>T | ENSP00000501920.1:p.Gly138= | |
| ENST00000678163.1:c.627G>T | ENSP00000502845.1:p.Gly209= | |
| ENST00000370695.6:c.627G>T | ENSP00000359729.4:p.Gly209= | |
| ENST00000370698.7:c.531G>T | ENSP00000359732.3:p.Gly177= | |
| ENST00000370701.5:c.471G>T | ENSP00000359735.1:p.Gly157= | |
| ENST00000627534.2:c.471G>T | ENSP00000486743.1:p.Gly157= | |
| NM_001042537.1:c.627G>T | NP_001036002.1:p.Gly209= | |
| NM_001177651.1:c.471G>T | NP_001171122.1:p.Gly157= | |
| NM_006359.2:c.531G>T | NP_006350.1:p.Gly177= | |
| XM_006724726.2:c.471G>T | XP_006724789.1:p.Gly157= | |
| XM_011531243.1:c.375G>T | XP_011529545.1:p.Gly125= | |
| NM_001330652.1:c.375G>T | NP_001317581.1:p.Gly125= | |
| XM_006724726.3:c.471G>T | XP_006724789.1:p.Gly157= | |
| XM_017029223.2:c.471G>T | XP_016884712.1:p.Gly157= | |
| XM_017029224.1:c.471G>T | XP_016884713.1:p.Gly157= | |
| XM_017029225.1:c.375G>T | XP_016884714.1:p.Gly125= | |
| NM_001177651.2:c.471G>T | NP_001171122.1:p.Gly157= | |
| NM_001330652.2:c.375G>T | NP_001317581.1:p.Gly125= | |
| NM_006359.3:c.531G>T | NP_006350.1:p.Gly177= | |
| NM_001042537.2:c.627G>T | NP_001036002.1:p.Gly209= | |
| NM_001379110.1:c.471G>T MANE Select | NP_001366039.1:p.Gly157= | |
| NM_001400909.1:c.471G>T | NP_001387838.1:p.Gly157= | |
| NM_001400910.1:c.471G>T | NP_001387839.1:p.Gly157= | |
| NM_001400911.1:c.471G>T | NP_001387840.1:p.Gly157= | |
| NM_001400912.1:c.471G>T | NP_001387841.1:p.Gly157= | |
| NM_001400913.1:c.375G>T | NP_001387842.1:p.Gly125= |