| NCBI GeneID : 11137 | NCBI : NM_007062.3 | NCBI : NP_008993.1 |
|---|---|---|
| Chromosome : 12 | Strand : + | |
| MANE Select : ENST00000412830 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | PWP1 | ENSG00000136045 | 107685799 | 107713162 |
|---|---|---|---|---|
| GTEx V9 | PWP1 | ENSG00000136045 | 107685731 | 107713167 |
| Gencode v40 | PWP1 | ENSG00000136045 | 107685798 | 107713162 |
| Gencode v26 (GTEx V9) | Gencode v40 | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| V9 |
Transcript ID | Exon Count |
Transcript Length |
Tx Length Rank |
CDS Length |
CDS Rank |
Exp Tx% |
Exp Rank |
MANE Match |
APPRIS | Transcript ID | Exon Count |
Transcript Length |
Tx Length Rank |
CDS Length |
CDS Rank |
MANE Match |
APPRIS |
| ☉ | ENST00000412830 | 15 | 2621 | 1 | 1506 | 1 | 99.61 | 1 | ☀ | P:1 | ENST00000412830 | 15 | 2549 | 1 | 1506 | 1 | ☀ | P:1 |
| ENST00000552760 | 7 | 851 | 3 | 444 | 3 | 0.27 | 2 | ENST00000552760 | 7 | 851 | 3 | 444 | 3 | |||||
| ENST00000541166 | 15 | 1722 | 2 | 1320 | 2 | 0.09 | 3 | ENST00000541166 | 15 | 1722 | 2 | 1320 | 2 | |||||
| ENST00000547120 | 4 | 543 | 5 | 0 | 5 | 0.03 | 4 | ENST00000547120 | 4 | 543 | 5 | 0 | 5 | |||||
| ENST00000547995 | 5 | 569 | 4 | 295 | 4 | 0.00 | 5 | ENST00000547995 | 5 | 569 | 4 | 295 | 4 | |||||