| NCBI GeneID : 56975 | NCBI : NM_020223.4 | NCBI : NP_064608.2 |
|---|---|---|
| Chromosome : 7 | Strand : + | |
| MANE Select : ENST00000313766 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | FAM20C | ENSG00000177706 | 192571 | 260772 |
|---|---|---|---|---|
| GTEx V9 | FAM20C | ENSG00000177706 | 192968 | 260745 |
| Gencode v40 | FAM20C | ENSG00000177706 | 192570 | 260772 |
| 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 |
| ☉ | ENST00000313766 | 10 | 2751 | 1 | 1755 | 1 | 80.25 | 1 | ☀ | P:1 | ENST00000313766 | 10 | 3176 | 1 | 1755 | 1 | ☀ | P:1 |
| ENST00000515795 | 7 | 2177 | 2 | 0 | 2 | 0.91 | 3 | ENST00000515795 | 7 | 2177 | 2 | 0 | 2 | |||||
| ENST00000512382 | 2 | 1018 | 3 | 0 | 2 | 0.19 | 5 | ENST00000512382 | 2 | 1018 | 3 | 0 | 2 | |||||
| ENST00000471328 | 2 | 554 | 4 | 0 | 2 | 18.13 | 2 | ENST00000471328 | 2 | 554 | 4 | 0 | 2 | |||||
| ENST00000477004 | 3 | 344 | 5 | 0 | 2 | 0.52 | 4 | ENST00000477004 | 3 | 344 | 5 | 0 | 2 | |||||