| NCBI GeneID : 8796 | NCBI : NM_144777.3 | NCBI : NP_659001.2 |
|---|---|---|
| Chromosome : 13 | Strand : + | |
| MANE Select : ENST00000349847 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | SCEL | ENSG00000136155 | 77535706 | 77645263 |
|---|---|---|---|---|
| GTEx V9 | SCEL | ENSG00000136155 | 77535673 | 77645263 |
| Gencode v40 | SCEL | ENSG00000136155 | 77535673 | 77645263 |
| 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 |
| ☉ | ENST00000377246 | 32 | 3081 | 2 | 2007 | 2 | 42.31 | 1 | A:2 | ENST00000377246 | 32 | 3081 | 3 | 2007 | 2 | A:2 | ||
| ENST00000349847 | 33 | 2386 | 3 | 2067 | 1 | 30.12 | 2 | ☀ | P:2 | ENST00000349847 | 33 | 3194 | 1 | 2067 | 1 | ☀ | P:2 | |
| ENST00000535157 | 31 | 3096 | 1 | 1941 | 3 | 15.43 | 3 | A:2 | ENST00000535157 | 31 | 3096 | 2 | 1941 | 3 | A:2 | |||
| ENST00000471491 | 19 | 2269 | 4 | 852 | 4 | 11.88 | 4 | ENST00000471491 | 19 | 2269 | 4 | 852 | 4 | |||||
| ENST00000469982 | 10 | 590 | 5 | 0 | 5 | 0.26 | 5 | ENST00000469982 | 10 | 590 | 5 | 0 | 5 | |||||