| NCBI GeneID : 29775 | NCBI : NM_014550.4 | NCBI : NP_055365.2 |
|---|---|---|
| Chromosome : 22 | Strand : - | |
| MANE Select : ENST00000251973 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | CARD10 | ENSG00000100065 | 37490362 | 37519415 |
|---|---|---|---|---|
| GTEx V8 | CARD10 | ENSG00000100065 | 37490361 | 37519542 |
| Gencode v40 | CARD10 | ENSG00000100065 | 37490361 | 37519542 |
| Gencode v26 (GTEx V8) | Gencode v40 | |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| V8 |
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 |
| ☉ | ENST00000251973 | 20 | 3934 | 2 | 3099 | 1 | 44.24 | 1 | ☀ | P:1 | ENST00000251973 | 20 | 4111 | 2 | 3099 | 1 | ☀ | P:1 |
| ENST00000467812 | 5 | 1910 | 6 | 0 | 6 | 22.49 | 2 | ENST00000467812 | 5 | 1910 | 6 | 0 | 6 | |||||
| ENST00000488141 | 8 | 2169 | 4 | 0 | 6 | 18.44 | 3 | ENST00000488141 | 8 | 2169 | 4 | 0 | 6 | |||||
| ENST00000403299 | 21 | 4113 | 1 | 3099 | 1 | 6.57 | 4 | P:1 | ENST00000403299 | 21 | 4113 | 1 | 3099 | 1 | P:1 | |||
| ENST00000406271 | 17 | 3127 | 3 | 2241 | 3 | 3.44 | 5 | ENST00000406271 | 17 | 3127 | 3 | 2241 | 3 | |||||
| ENST00000476871 | 3 | 583 | 7 | 0 | 6 | 1.35 | 6 | ENST00000476871 | 3 | 583 | 7 | 0 | 6 | |||||
| ENST00000433485 | 6 | 578 | 8 | 578 | 5 | 1.18 | 7 | ENST00000433485 | 6 | 578 | 8 | 578 | 5 | |||||
| ENST00000437756 | 15 | 2140 | 5 | 1441 | 4 | 1.04 | 8 | ENST00000437756 | 15 | 2140 | 5 | 1441 | 4 | |||||
| ENST00000486118 | 3 | 546 | 10 | 0 | 6 | 0.99 | 9 | ENST00000486118 | 3 | 546 | 10 | 0 | 6 | |||||
| ENST00000494166 | 3 | 560 | 9 | 0 | 6 | 0.26 | 10 | ENST00000494166 | 3 | 560 | 9 | 0 | 6 | |||||