NCBI GeneID : 57569 | NCBI : NM_001384657.1 | NCBI : NP_001371586.1 |
---|---|---|
Chromosome : 11 | Strand : - | |
MANE Select : ENST00000683387 | MANE Plus Clinical : |
Gene Symbol | Ensembl Gene ID | Start | End | |
MANE | ARHGAP20 | ENSG00000137727 | 110577043 | 110712437 |
---|---|---|---|---|
GTEx V8 | ARHGAP20 | ENSG00000137727 | 110577041 | 110713189 |
Gencode v40 | ARHGAP20 | ENSG00000137727 | 110577041 | 110713189 |
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 |
☉ | ENST00000528829 | 15 | 5880 | 5 | 3468 | 4 | 68.40 | 1 | A:2 | ENST00000528829 | 15 | 5880 | 6 | 3468 | 5 | A:2 | ||
ENST00000260283 | 16 | 6189 | 1 | 3576 | 1 | 23.74 | 2 | P:4 | ENST00000260283 | 16 | 6189 | 1 | 3576 | 1 | P:4 | |||
ENST00000524756 | 15 | 6180 | 2 | 3507 | 2 | 5.20 | 3 | A:2 | ENST00000524756 | 15 | 6180 | 2 | 3507 | 3 | A:2 | |||
ENST00000529591 | 6 | 2623 | 6 | 2196 | 6 | 2.06 | 4 | ENST00000529591 | 6 | 2623 | 7 | 2196 | 7 | |||||
ENST00000527598 | 15 | 5998 | 4 | 3468 | 4 | 0.58 | 5 | A:2 | ENST00000527598 | 15 | 5998 | 5 | 3468 | 5 | A:2 | |||
ENST00000533353 | 16 | 6066 | 3 | 3498 | 3 | 0.01 | 6 | A:2 | ENST00000533353 | 16 | 6066 | 4 | 3498 | 4 | A:2 |
Gencode v26 (GTEx V8) | Gencode v40 | |||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
V8 |
No Match Transcript ID |
Exon Count |
Transcript Length |
Tx Length Rank |
CDS Length |
CDS Rank |
Exp Tx% |
Exp Rank |
MANE Match |
APPRIS | No Match Transcript ID |
Exon Count |
Transcript Length |
Tx Length Rank |
CDS Length |
CDS Rank |
MANE Match |
APPRIS |
ENST00000000000 | ENST00000683387 | 15 | 6109 | 3 | 3576 | 1 | ☀ | P:4 |