| NCBI GeneID : 4778 | NCBI : NM_001136023.3 | NCBI : NP_001129495.1 |
|---|---|---|
| Chromosome : 12 | Strand : - | |
| MANE Select : ENST00000435572 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | NFE2 | ENSG00000123405 | 54292111 | 54301015 |
|---|---|---|---|---|
| GTEx V9 | NFE2 | ENSG00000123405 | 54292110 | 54301121 |
| Gencode v40 | NFE2 | ENSG00000123405 | 54292110 | 54301015 |
| 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 |
| ☉ | ENST00000435572 | 3 | 1762 | 2 | 1122 | 1 | 96.03 | 1 | ☀ | P:1 | ENST00000435572 | 3 | 1656 | 3 | 1122 | 1 | ☀ | P:1 |
| ENST00000312156 | 3 | 1658 | 3 | 1122 | 1 | 1.82 | 2 | P:1 | ENST00000312156 | 3 | 1658 | 2 | 1122 | 1 | P:1 | |||
| ENST00000540264 | 2 | 1833 | 1 | 1122 | 1 | 1.75 | 3 | P:1 | ENST00000540264 | 2 | 1833 | 1 | 1122 | 1 | P:1 | |||
| ENST00000553198 | 3 | 1208 | 5 | 1031 | 5 | 0.41 | 4 | ENST00000553198 | 3 | 1208 | 5 | 1031 | 5 | |||||
| ENST00000553070 | 4 | 1523 | 4 | 1122 | 1 | 0.00 | 5 | P:1 | ENST00000553070 | 4 | 1523 | 4 | 1122 | 1 | P:1 | |||