| NCBI GeneID : 1032 | NCBI : NM_001800.4 | NCBI : NP_001791.1 |
|---|---|---|
| Chromosome : 19 | Strand : - | |
| MANE Select : ENST00000393599 | MANE Plus Clinical : |
| Gene Symbol | Ensembl Gene ID | Start | End | |
| MANE | CDKN2D | ENSG00000129355 | 10566460 | 10568979 |
|---|---|---|---|---|
| GTEx V9 | CDKN2D | ENSG00000129355 | 10566461 | 10569059 |
| Gencode v40 | CDKN2D | ENSG00000129355 | 10566459 | 10569059 |
| 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 |
| ☉ | ENST00000393599 | 2 | 1422 | 1 | 501 | 1 | 99.03 | 1 | ☀ | P:1 | ENST00000393599 | 2 | 1425 | 1 | 501 | 1 | ☀ | P:1 |
| ENST00000335766 | 3 | 1086 | 2 | 501 | 1 | 0.97 | 2 | P:1 | ENST00000335766 | 3 | 1086 | 2 | 501 | 1 | P:1 | |||