| NCBI GeneID : 3241 | NCBI : NM_002149.4 | NCBI : NP_002140.2 |
|---|---|---|
| Chromosome : 2 | Strand : + | |
| MANE Select : ENST00000307845 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | HPCAL1 | ENSG00000115756 | 10302904 | 10427604 |
|---|---|---|---|---|
| GTEx V9 | HPCAL1 | ENSG00000115756 | 10302888 | 10427617 |
| Gencode v40 | HPCAL1 | ENSG00000115756 | 10302888 | 10427617 |
| 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 |
| ☉ | ENST00000307845 | 5 | 1751 | 4 | 582 | 1 | 86.81 | 1 | ☀ | P:1 | ENST00000307845 | 5 | 1749 | 4 | 582 | 1 | ☀ | P:1 |
| ENST00000381765 | 6 | 1904 | 3 | 582 | 1 | 6.22 | 2 | P:1 | ENST00000381765 | 6 | 1904 | 3 | 582 | 1 | P:1 | |||
| ENST00000613496 | 5 | 1547 | 5 | 582 | 1 | 3.20 | 3 | P:1 | ENST00000613496 | 5 | 1547 | 5 | 582 | 1 | P:1 | |||
| ENST00000419810 | 8 | 4781 | 1 | 528 | 6 | 2.56 | 4 | ENST00000419810 | 8 | 4781 | 1 | 528 | 6 | |||||
| ENST00000620771 | 5 | 1941 | 2 | 582 | 1 | 0.71 | 5 | P:1 | ENST00000620771 | 5 | 1941 | 2 | 582 | 1 | P:1 | |||
| ENST00000423674 | 4 | 586 | 8 | 90 | 8 | 0.48 | 6 | ENST00000423674 | 4 | 586 | 8 | 90 | 8 | |||||
| ENST00000422133 | 4 | 587 | 7 | 310 | 7 | 0.01 | 7 | ENST00000422133 | 4 | 587 | 7 | 310 | 7 | |||||
| ENST00000622018 | 5 | 1535 | 6 | 582 | 1 | 0.01 | 8 | P:1 | ENST00000622018 | 5 | 1535 | 6 | 582 | 1 | P:1 | |||