Linked Data
ClinVar Variation Id:
157632
ClinVar RCV Id:
RCV000162257
dbSNP Id:
rs2301826
ExAC:
15:91525197 C / T
gnomAD v2:
15-91525197-C-T
gnomAD v3:
15-90981967-C-T
gnomAD v4:
15-90981967-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.90981967C>T , CM000677.2:g.90981967C>T | GRCh38 |
| NC_000015.9:g.91525197C>T , CM000677.1:g.91525197C>T | GRCh37 |
| NC_000015.8:g.89326201C>T | NCBI36 |
| NG_050647.1:g.17685G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000394249.8:c.282G>A (PRC1) MANE Select | ENSP00000377793.3:p.Thr94= | |
| ENST00000643536.1:c.*245G>A | ENSP00000494429.1:n.*245G>A | |
| ENST00000647331.1:c.*245G>A | ENSP00000493953.1:n.*245G>A | |
| ENST00000361188.9:c.282G>A (PRC1) | ENSP00000354679.5:p.Thr94= | |
| ENST00000394249.7:c.282G>A (PRC1) | ENSP00000377793.3:p.Thr94= | |
| ENST00000417173.6:n.269G>A (PRC1) | ||
| ENST00000442656.6:c.159G>A (PRC1) | ENSP00000409549.2:p.Thr53= | |
| ENST00000553494.5:n.401G>A (PRC1) | ||
| ENST00000555745.5:n.524G>A (PRC1) | ||
| ENST00000555791.5:n.579G>A (PRC1) | ||
| ENST00000557763.5:n.369G>A (PRC1) | ||
| ENST00000557905.5:c.159G>A (PRC1) | ENSP00000453455.1:p.Thr53= | |
| ENST00000559811.1:c.327G>A (PRC1) | ENSP00000453117.1:p.Thr109= | |
| ENST00000560605.1:n.119G>A (PRC1) | ||
| NM_001267580.1:c.159G>A (PRC1) | NP_001254509.1:p.Thr53= | |
| NM_003981.3:c.282G>A (PRC1) | NP_003972.1:p.Thr94= | |
| NM_199413.2:c.282G>A (PRC1) | NP_955445.1:p.Thr94= | |
| NR_051984.1:n.323C>T (PRC1-AS1) | ||
| XM_005254987.1:c.282G>A (PRC1) | XP_005255044.1:p.Thr94= | |
| XM_006720759.1:c.282G>A (PRC1) | XP_006720822.1:p.Thr94= | |
| XM_006720760.1:c.282G>A (PRC1) | XP_006720823.1:p.Thr94= | |
| XM_011522187.1:c.282G>A (PRC1) | XP_011520489.1:p.Thr94= | |
| XM_011522188.1:c.282G>A (PRC1) | XP_011520490.1:p.Thr94= | |
| XM_011522189.1:c.282G>A (PRC1) | XP_011520491.1:p.Thr94= | |
| XM_011522190.1:c.282G>A (PRC1) | XP_011520492.1:p.Thr94= | |
| XM_011522191.1:c.282G>A (PRC1) | XP_011520493.1:p.Thr94= | |
| XM_011522192.1:c.282G>A (PRC1) | XP_011520494.1:p.Thr94= | |
| XM_005254987.3:c.282G>A (PRC1) | XP_005255044.1:p.Thr94= | |
| XM_006720759.2:c.282G>A (PRC1) | XP_006720822.1:p.Thr94= | |
| XM_006720760.2:c.282G>A (PRC1) | XP_006720823.1:p.Thr94= | |
| XM_011522187.2:c.282G>A (PRC1) | XP_011520489.1:p.Thr94= | |
| XM_011522188.3:c.282G>A (PRC1) | XP_011520490.1:p.Thr94= | |
| XM_011522189.2:c.282G>A (PRC1) | XP_011520491.1:p.Thr94= | |
| XM_011522190.3:c.282G>A (PRC1) | XP_011520492.1:p.Thr94= | |
| XM_011522191.3:c.282G>A (PRC1) | XP_011520493.1:p.Thr94= | |
| XM_011522192.2:c.282G>A (PRC1) | XP_011520494.1:p.Thr94= | |
| XM_017022712.2:c.282G>A (PRC1) | XP_016878201.1:p.Thr94= | |
| XM_017022713.2:c.282G>A (PRC1) | XP_016878202.1:p.Thr94= | |
| XM_017022714.2:c.126G>A (PRC1) | XP_016878203.1:p.Thr42= | |
| XM_017022715.2:c.126G>A (PRC1) | XP_016878204.1:p.Thr42= | |
| XM_017022716.2:c.282G>A (PRC1) | XP_016878205.1:p.Thr94= | |
| XM_017022717.1:c.126G>A (PRC1) | XP_016878206.1:p.Thr42= | |
| NM_003981.4:c.282G>A (PRC1) MANE Select | NP_003972.2:p.Thr94= | |
| NM_001267580.2:c.159G>A (PRC1) | NP_001254509.2:p.Thr53= | |
| NM_199413.3:c.282G>A (PRC1) | NP_955445.2:p.Thr94= |