| NCBI GeneID : 10452 | NCBI : NM_001128917.2 | NCBI : NP_001122389.1 |
|---|---|---|
| Chromosome : 19 | Strand : + | |
| MANE Select : ENST00000426677 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | TOMM40 | ENSG00000130204 | 44891254 | 44903689 |
|---|---|---|---|---|
| GTEx V8 | TOMM40 | ENSG00000130204 | 44890568 | 44903689 |
| Gencode v40 | TOMM40 | ENSG00000130204 | 44890568 | 44903689 |
| 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 |
| ☉ | ENST00000405636 | 10 | 1709 | 3 | 1086 | 1 | 60.13 | 1 | P:1 | ENST00000405636 | 10 | 1709 | 3 | 1086 | 1 | P:1 | ||
| ENST00000252487 | 10 | 1707 | 4 | 1086 | 1 | 23.90 | 2 | P:1 | ENST00000252487 | 10 | 1707 | 4 | 1086 | 1 | P:1 | |||
| ENST00000592434 | 9 | 3415 | 1 | 990 | 4 | 9.66 | 3 | ENST00000592434 | 9 | 3415 | 1 | 990 | 4 | |||||
| ENST00000426677 | 9 | 1725 | 2 | 1086 | 1 | 4.59 | 4 | ☀ | P:1 | ENST00000426677 | 9 | 1768 | 2 | 1086 | 1 | ☀ | P:1 | |
| ENST00000592041 | 6 | 707 | 6 | 506 | 6 | 1.42 | 5 | ENST00000592041 | 6 | 707 | 6 | 506 | 6 | |||||
| ENST00000589649 | 6 | 731 | 5 | 644 | 5 | 0.28 | 6 | ENST00000589649 | 6 | 731 | 5 | 644 | 5 | |||||
| ENST00000589253 | 2 | 207 | 7 | 110 | 7 | 0.02 | 7 | ENST00000589253 | 2 | 207 | 7 | 110 | 7 | |||||