| NCBI GeneID : 80162 | NCBI : NM_025092.5 | NCBI : NP_079368.3 |
|---|---|---|
| Chromosome : 11 | Strand : + | |
| MANE Select : ENST00000409548 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | PGGHG | ENSG00000142102 | 289126 | 296107 |
|---|---|---|---|---|
| GTEx V8 | PGGHG | ENSG00000142102 | 289134 | 296107 |
| Gencode v40 | PGGHG | ENSG00000142102 | 289125 | 296107 |
| Gencode v26 (GTEx V8) | Gencode v40 | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| V8 |
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 |
| ENST00000476372 | 8 | 2879 | 5 | 0 | 6 | 23.36 | 1 | ENST00000476372 | 8 | 2879 | 5 | 0 | 6 | |||||
| ☉ | ENST00000409479 | 13 | 3062 | 3 | 2295 | 1 | 21.65 | 2 | A:2 | ENST00000409479 | 13 | 3062 | 3 | 2295 | 1 | A:2 | ||
| ENST00000529087 | 3 | 745 | 6 | 0 | 6 | 16.48 | 3 | ENST00000529087 | 3 | 745 | 6 | 0 | 6 | |||||
| ENST00000409548 | 14 | 3687 | 2 | 2214 | 2 | 14.35 | 4 | ☀ | P:2 | ENST00000409548 | 14 | 3699 | 2 | 2214 | 2 | ☀ | P:2 | |
| ENST00000474221 | 11 | 4418 | 1 | 0 | 6 | 12.31 | 5 | ENST00000474221 | 11 | 4418 | 1 | 0 | 6 | |||||
| ENST00000409655 | 13 | 2963 | 4 | 1470 | 3 | 5.20 | 6 | ENST00000409655 | 13 | 2963 | 4 | 1470 | 3 | |||||
| ENST00000397660 | 5 | 578 | 8 | 578 | 5 | 4.34 | 7 | ENST00000397660 | 5 | 578 | 8 | 578 | 5 | |||||
| ENST00000482937 | 6 | 734 | 7 | 611 | 4 | 2.31 | 8 | ENST00000482937 | 6 | 734 | 7 | 611 | 4 | |||||