chr2:29192774:> Detail (hg38) (ALK)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chr2:29,415,640-30,144,432 |
| hg38 | chr2:29,192,774-29,921,566 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
[No Data.]
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| Show details | |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
| Disease | Drug | EL | ET | ED | CS | VO | TR | Pubmed | Links |
|---|---|---|---|---|---|---|---|---|---|
| lung non-small cell carcinoma | Ceritinib | B |
Predictive
|
Supports
|
Sensitivity/Response | Somatic | 4 | 24670165 | Detail |
DisGeNET
[No Data.]
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| In a phase 1 clinical trial (NCT01283516) 130 patients with advanced cancers all harboring ALK alter... | CIViC Evidence | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- Genome
- hg38
- Position
- chr2:29,192,774-29,921,566
- Variant Type
- snv
- Variant (CIViC) (CIViC Variant)
- MUTATION
- Transcript 1 (CIViC Variant)
- ENST00000389048.3
- Variant URL (CIViC Variant)
- https://civic.genome.wustl.edu/links/variants/512
Genome browser