| NCBI GeneID : 3146 | NCBI : NM_002128.7 | NCBI : NP_002119.1 |
|---|---|---|
| Chromosome : 13 | Strand : - | |
| MANE Select : ENST00000341423 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | HMGB1 | ENSG00000189403 | 30456704 | 30465936 |
|---|---|---|---|---|
| GTEx V9 | HMGB1 | ENSG00000189403 | 30456703 | 30617597 |
| Gencode v40 | HMGB1 | ENSG00000189403 | 30456703 | 30617597 |
| 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 |
| ENST00000326004 | 5 | 821 | 6 | 477 | 5 | 0.21 | 6 | ENST00000326004 | 5 | 821 | 6 | 477 | 5 | |||||
| ENST00000339872 | 5 | 2319 | 3 | 648 | 1 | 3.08 | 2 | P:1 | ENST00000339872 | 5 | 2319 | 3 | 648 | 1 | P:1 | |||
| ENST00000399494 | 5 | 1282 | 5 | 648 | 1 | 0.97 | 4 | P:1 | ENST00000399494 | 5 | 1282 | 5 | 648 | 1 | P:1 | |||
| ENST00000399489 | 5 | 1727 | 4 | 477 | 5 | 1.41 | 3 | ENST00000399489 | 5 | 1727 | 4 | 477 | 5 | |||||
| ENST00000490788 | 2 | 425 | 8 | 0 | 7 | 0.06 | 7 | ENST00000490788 | 2 | 425 | 8 | 0 | 7 | |||||
| ENST00000405805 | 5 | 4199 | 2 | 648 | 1 | 0.69 | 5 | P:1 | ENST00000405805 | 5 | 4199 | 2 | 648 | 1 | P:1 | |||
| ☉ | ENST00000341423 | 5 | 5485 | 1 | 648 | 1 | 93.57 | 1 | ☀ | P:1 | ENST00000341423 | 5 | 5456 | 1 | 648 | 1 | ☀ | P:1 |
| ENST00000468384 | 2 | 503 | 7 | 0 | 7 | 0.02 | 8 | ENST00000468384 | 2 | 503 | 7 | 0 | 7 | |||||