| NCBI GeneID : 3052 | NCBI : NM_005333.5 | NCBI : NP_005324.3 |
|---|---|---|
| Chromosome : X | Strand : + | |
| MANE Select : ENST00000380762 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | HCCS | ENSG00000004961 | 11111332 | 11123086 |
|---|---|---|---|---|
| GTEx V9 | HCCS | ENSG00000004961 | 11111300 | 11123078 |
| Gencode v40 | HCCS | ENSG00000004961 | 11111300 | 11123086 |
| 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 |
| ☉ | ENST00000321143 | 7 | 2277 | 1 | 807 | 1 | 52.75 | 1 | P:1 | ENST00000321143 | 7 | 2277 | 2 | 807 | 1 | P:1 | ||
| ENST00000380762 | 7 | 1072 | 2 | 807 | 1 | 46.43 | 2 | ☀ | P:1 | ENST00000380762 | 7 | 2312 | 1 | 807 | 1 | ☀ | P:1 | |
| ENST00000380763 | 7 | 1000 | 3 | 807 | 1 | 0.82 | 3 | P:1 | ENST00000380763 | 7 | 1000 | 3 | 807 | 1 | P:1 | |||