Linked Data
ClinVar Variation Id:
430566
ClinVar RCV Id:
RCV000493080
dbSNP Id:
rs1131692029
gnomAD v4:
X-22219058-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.22219058G>A , CM000685.2:g.22219058G>A | GRCh38 |
| NC_000023.10:g.22237175G>A , CM000685.1:g.22237175G>A | GRCh37 |
| NC_000023.9:g.22147096G>A | NCBI36 |
| NG_007563.2:g.191255G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682888.1:c.277G>A (PHEX) | ENSP00000508003.1:p.Gly93Arg | |
| ENST00000683162.1:c.277G>A (PHEX) | ENSP00000508059.1:p.Gly93Arg | |
| ENST00000683289.1:c.277G>A (PHEX) | ENSP00000508195.1:p.Gly93Arg | |
| ENST00000683917.1:n.507G>A (PHEX) | ||
| ENST00000684356.1:c.277G>A (PHEX) | ENSP00000507619.1:p.Gly93Arg | |
| ENST00000684745.1:n.1397G>A (PHEX) | ||
| ENST00000379374.5:c.1723G>A (PHEX) MANE Select | ENSP00000368682.4:p.Gly575Arg | |
| ENST00000379374.4:c.1723G>A (PHEX) | ENSP00000368682.4:p.Gly575Arg | |
| NM_000444.5:c.1723G>A (PHEX) | NP_000435.3:p.Gly575Arg | |
| NM_001282754.1:c.1723G>A (PHEX) | NP_001269683.1:p.Gly575Arg | |
| XM_011545533.1:c.967G>A (PHEX) | XP_011543835.1:p.Gly323Arg | |
| XM_011545534.1:c.967G>A (PHEX) | XP_011543836.1:p.Gly323Arg | |
| XM_011545536.1:c.616G>A (PHEX) | XP_011543838.1:p.Gly206Arg | |
| NR_073010.2:n.1048+8412C>T (PTCHD1-AS) | ||
| XM_011545536.2:c.616G>A (PHEX) | XP_011543838.1:p.Gly206Arg | |
| XM_017029579.1:c.967G>A (PHEX) | XP_016885068.1:p.Gly323Arg | |
| XM_024452390.1:c.1432G>A (PHEX) | XP_024308158.1:p.Gly478Arg | |
| XR_001755695.1:n.2563G>A (PHEX) | ||
| NM_000444.6:c.1723G>A (PHEX) MANE Select | NP_000435.3:p.Gly575Arg | |
| NM_001282754.2:c.1723G>A (PHEX) | NP_001269683.1:p.Gly575Arg |