| NCBI GeneID : 10042 | NCBI : NM_001003681.3 | NCBI : NP_001003681.1 |
|---|---|---|
| Chromosome : 22 | Strand : + | |
| MANE Select : ENST00000216106 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | HMGXB4 | ENSG00000100281 | 35257493 | 35295807 |
|---|---|---|---|---|
| GTEx V9 | HMGXB4 | ENSG00000100281 | 35257451 | 35295807 |
| Gencode v40 | HMGXB4 | ENSG00000100281 | 35257451 | 35295807 |
| 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 |
| ENST00000216106 | 11 | 4047 | 2 | 1806 | 1 | 21.35 | 3 | ☀ | P:1 | ENST00000216106 | 11 | 4095 | 2 | 1806 | 1 | ☀ | P:1 | |
| ENST00000418170 | 12 | 4216 | 1 | 279 | 4 | 32.57 | 2 | ENST00000418170 | 12 | 4216 | 1 | 279 | 4 | |||||
| ENST00000498212 | 3 | 778 | 6 | 0 | 5 | 1.99 | 5 | ENST00000498212 | 3 | 778 | 6 | 0 | 5 | |||||
| ☉ | ENST00000420166 | 4 | 1257 | 4 | 855 | 2 | 34.14 | 1 | ENST00000420166 | 4 | 1257 | 4 | 855 | 2 | ||||
| ENST00000455359 | 5 | 1325 | 3 | 852 | 3 | 8.55 | 4 | ENST00000455359 | 5 | 1325 | 3 | 852 | 3 | |||||
| ENST00000466438 | 2 | 575 | 7 | 0 | 5 | 1.24 | 6 | ENST00000466438 | 2 | 575 | 7 | 0 | 5 | |||||
| ENST00000498325 | 4 | 867 | 5 | 0 | 5 | 0.15 | 7 | ENST00000498325 | 4 | 867 | 5 | 0 | 5 | |||||
| ENST00000464480 | 3 | 559 | 8 | 0 | 5 | 0.01 | 8 | ENST00000464480 | 3 | 559 | 8 | 0 | 5 | |||||