| NCBI GeneID : 5774 | NCBI : NM_002829.4 | NCBI : NP_002820.3 |
|---|---|---|
| Chromosome : 9 | Strand : - | |
| MANE Select : ENST00000374541 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | PTPN3 | ENSG00000070159 | 109375700 | 109498307 |
|---|---|---|---|---|
| GTEx V9 | PTPN3 | ENSG00000070159 | 109375465 | 109498313 |
| Gencode v40 | PTPN3 | ENSG00000070159 | 109375465 | 109498313 |
| 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 |
| ENST00000497739 | 5 | 781 | 5 | 0 | 5 | 50.64 | 1 | ENST00000497739 | 5 | 781 | 5 | 0 | 5 | |||||
| ☉ | ENST00000374541 | 26 | 6703 | 4 | 2742 | 1 | 23.01 | 2 | ☀ | P:1 | ENST00000374541 | 26 | 6704 | 4 | 2742 | 1 | ☀ | P:1 |
| ENST00000446349 | 20 | 8630 | 2 | 2214 | 4 | 12.64 | 3 | ENST00000446349 | 20 | 8630 | 2 | 2214 | 4 | |||||
| ENST00000447271 | 2 | 587 | 6 | 0 | 5 | 7.22 | 4 | ENST00000447271 | 2 | 587 | 6 | 0 | 5 | |||||
| ENST00000262539 | 26 | 6832 | 3 | 2520 | 2 | 4.12 | 5 | ENST00000262539 | 26 | 6832 | 3 | 2520 | 2 | |||||
| ENST00000412145 | 21 | 8765 | 1 | 2349 | 3 | 2.38 | 6 | ENST00000412145 | 21 | 8765 | 1 | 2349 | 3 | |||||