| NCBI GeneID : 94134 | NCBI : NM_018287.7 | NCBI : NP_060757.4 |
|---|---|---|
| Chromosome : 10 | Strand : - | |
| MANE Select : ENST00000344936 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | ARHGAP12 | ENSG00000165322 | 31805398 | 31928831 |
|---|---|---|---|---|
| GTEx V8 | ARHGAP12 | ENSG00000165322 | 31805403 | 31928876 |
| Gencode v40 | ARHGAP12 | ENSG00000165322 | 31805397 | 31928876 |
| 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 |
| ENST00000493008 | 3 | 2334 | 7 | 0 | 7 | 27.79 | 1 | ENST00000493008 | 3 | 2334 | 7 | 0 | 7 | |||||
| ☉ | ENST00000375250 | 18 | 4914 | 3 | 2451 | 3 | 19.28 | 2 | A:1 | ENST00000375250 | 18 | 4914 | 4 | 2451 | 3 | A:1 | ||
| ENST00000497085 | 2 | 1641 | 8 | 0 | 7 | 14.36 | 3 | ENST00000497085 | 2 | 1641 | 8 | 0 | 7 | |||||
| ENST00000375245 | 19 | 4958 | 2 | 2400 | 4 | 13.18 | 4 | A:1 | ENST00000375245 | 19 | 4958 | 3 | 2400 | 4 | A:1 | |||
| ENST00000492028 | 11 | 3227 | 6 | 0 | 7 | 8.03 | 5 | ENST00000492028 | 11 | 3227 | 6 | 0 | 7 | |||||
| ENST00000311380 | 16 | 4625 | 4 | 2385 | 5 | 7.21 | 6 | A:1 | ENST00000311380 | 16 | 4625 | 5 | 2385 | 5 | A:1 | |||
| ENST00000396144 | 19 | 5084 | 1 | 2526 | 2 | 6.22 | 7 | P:4 | ENST00000396144 | 19 | 5084 | 1 | 2526 | 2 | P:4 | |||
| ENST00000344936 | 20 | 4128 | 5 | 2541 | 1 | 2.15 | 8 | ☀ | A:1 | ENST00000344936 | 20 | 5060 | 2 | 2541 | 1 | ☀ | A:1 | |
| ENST00000497103 | 7 | 732 | 9 | 0 | 7 | 1.43 | 9 | ENST00000497103 | 7 | 732 | 9 | 0 | 7 | |||||
| ENST00000454919 | 7 | 586 | 10 | 586 | 6 | 0.37 | 10 | ENST00000454919 | 7 | 586 | 10 | 586 | 6 | |||||