| NCBI GeneID : 56941 | NCBI : NM_020187.3 | NCBI : NP_064572.2 |
|---|---|---|
| Chromosome : 3 | Strand : + | |
| MANE Select : ENST00000383463 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | HMCES | ENSG00000183624 | 129278870 | 129306186 |
|---|---|---|---|---|
| GTEx V9 | HMCES | ENSG00000183624 | 129278827 | 129306186 |
| Gencode v40 | HMCES | ENSG00000183624 | 129278827 | 129306186 |
| 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 |
| ☉ | ENST00000383463 | 7 | 2515 | 1 | 1065 | 1 | 95.16 | 1 | ☀ | P:1 | ENST00000383463 | 7 | 2485 | 1 | 1065 | 1 | ☀ | P:1 |
| ENST00000389735 | 7 | 1763 | 3 | 1065 | 1 | 0.27 | 4 | P:1 | ENST00000389735 | 7 | 1763 | 3 | 1065 | 1 | P:1 | |||
| ENST00000417226 | 6 | 1490 | 4 | 939 | 4 | 3.05 | 2 | ENST00000417226 | 6 | 1490 | 4 | 939 | 4 | |||||
| ENST00000502878 | 7 | 1952 | 2 | 1065 | 1 | 1.42 | 3 | P:1 | ENST00000502878 | 7 | 1952 | 2 | 1065 | 1 | P:1 | |||
| ENST00000509551 | 6 | 774 | 6 | 700 | 6 | 0.00 | 8 | ENST00000509551 | 6 | 774 | 6 | 700 | 6 | |||||
| ENST00000509042 | 6 | 948 | 5 | 847 | 5 | 0.04 | 5 | ENST00000509042 | 6 | 948 | 5 | 847 | 5 | |||||
| ENST00000510314 | 4 | 599 | 8 | 550 | 7 | 0.02 | 7 | ENST00000510314 | 4 | 599 | 8 | 550 | 7 | |||||
| ENST00000511665 | 4 | 643 | 7 | 421 | 8 | 0.04 | 6 | ENST00000511665 | 4 | 643 | 7 | 421 | 8 | |||||