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- Gene Symbol
- NAPA
- Assay Reference Genome
Location
Chr.19:47487986 on build GRCh38- Cytoband
Genomic Map
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Target Gene Details
Entrez Gene ID: | 8775 |
Gene Name: | NSF attachment protein alpha |
Gene Aliases: |
SNAPA |
Location: |
Chr.19:47484530-47515063 on Build GRCh38 |
Assay Gene Location: | Within Exon 12 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NAPA | NM_003827.4 | 11 | 1313 | NP_003818.2 |
| NR_038456.2 | ||||
| NR_038457.2 | 9 | 1116 | ||
| XM_011527436.2 | 11 | 1163 | XP_011525738.1 | |
| AA542963.1 | ||||
| AA807920.1 | ||||
| AK098401.1 | 11 | 1341 | ||
| AK123456.1 | 1 | 1534 | ||
| AK126519.1 | 5 | 3550 | ||
| AW206113.1 | ||||
| BC001165.1 | 11 | 1280 | AAH01165.1 | |
| BC007432.2 | 11 | 1271 | AAH07432.1 | |
| BC028234.1 | 11 | 1326 | AAH28234.1 | |
| BC091511.1 | 11 | 1287 | AAH91511.1 | |
| BU168063.1 | 6 | 746 | ||
| U39412.1 | AAC80170.1 |
Target Gene Details
Entrez Gene ID: | 100505681 |
Gene Name: | NAPA antisense RNA 1 |
Gene Aliases: |
- |
Location: |
Chr.19:47484282-47501597 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NAPA-AS1 | NR_038452.1 | |||
| AK057858.1 | ||||
| BG035979.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2025-12-01, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv428366 | Chr.19:47354499 - 47522248 on Build GRCh38 | Loss |
 NAPA
SLC8A2
MEIS3
KPTN
NAPA-AS1
DHX34
ZNF541
|
| nsv1056887 | Chr.19:47481963 - 47527369 on Build GRCh38 | Gain |
NAPA
KPTN
NAPA-AS1
ZNF541
|
| nsv579888 | Chr.19:47428355 - 47658874 on Build GRCh38 | Gain |
NAPA
SLC8A2
KPTN
BICRA
NAPA-AS1
BICRA-AS2
ZNF541
|
| nsv953591 | Chr.19:47486744 - 47500943 on Build GRCh38 | Deletion |
NAPA
NAPA-AS1
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs114963766,rs73940857] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Exonic
Intronic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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