| NCBI GeneID : 57190 | NCBI : NM_020451.3 | NCBI : NP_065184.2 |
|---|---|---|
| Chromosome : 1 | Strand : + | |
| MANE Select : ENST00000361547 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | SELENON | ENSG00000162430 | 25800193 | 25818221 |
|---|---|---|---|---|
| GTEx V9 | SELENON | ENSG00000162430 | 25800175 | 25818224 |
| Gencode v40 | SELENON | ENSG00000162430 | 25800192 | 25818221 |
| 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 |
| ☉ | ENST00000361547 | 13 | 4334 | 1 | 1773 | 1 | 73.33 | 1 | ☀ | A:2 | ENST00000361547 | 13 | 4314 | 1 | 1773 | 1 | ☀ | A:2 |
| ENST00000374315 | 12 | 4212 | 3 | 1671 | 2 | 24.14 | 2 | P:2 | ENST00000374315 | 12 | 4212 | 2 | 1671 | 2 | P:2 | |||
| ENST00000494537 | 5 | 812 | 4 | 0 | 4 | 1.43 | 3 | ENST00000494537 | 13 | 2032 | 3 | 1467 | 4 | |||||
| ENST00000354177 | 13 | 4227 | 2 | 1671 | 2 | 1.10 | 4 | A:2 | ENST00000354177 | 12 | 1602 | 4 | 1602 | 3 | A:2 | |||