HNF1A-AS1 HNF1A antisense RNA 1
Information
- Symbol
- HNF1A-AS1
- Type
- ncRNA
- Description
- HNF1A antisense RNA 1
- Entrez Gene ID
- 283460
- Genome
- hg19
- Position
- chr12:121,400,602-121,418,734
- Genome
- hg38
- Position
- chr12:120,962,799-120,980,931
- HGNC
- HGNC:26785 HGNC
- Ensembl
- ENSG00000241388 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
0 |
 |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | C12orf27 |
| SYNONYM | HAS1 |
| SYNONYM | HASTER |
| SYNONYM | NCRNA00262 |
| HGNC | HGNC:26785 HGNC |
| Ensembl | ENSG00000241388 Ensembl |
| AllianceGenome | HGNC:26785 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000646404.1 | hg38 | chr12 | 120,965,660 | 120,979,747 | 14,088 |
| ENST00000647473.1 | hg38 | chr12 | 120,962,799 | 120,980,931 | 18,133 |
| ENST00000701967.1 | hg38 | chr12 | 120,965,659 | 120,979,713 | 14,055 |
| ENST00000701238.1 | hg38 | chr12 | 120,965,659 | 120,980,968 | 15,310 |
| ENST00000537361.1 | hg38 | chr12 | 120,968,613 | 120,980,906 | 12,294 |
| ENST00000433033.3 | hg38 | chr12 | 120,970,024 | 120,979,747 | 9,724 |
| ENST00000535301.2 | hg38 | chr12 | 120,974,375 | 120,980,965 | 6,591 |
| ENST00000619441.1 | hg38 | chr12 | 120,941,728 | 120,980,771 | 39,044 |
| ENST00000619441.1 | hg19 | chr12 | 121,379,531 | 121,418,574 | 39,044 |
| ENST00000647473.1 | hg19 | chr12 | 121,400,602 | 121,418,734 | 18,133 |
| ENST00000701967.1 | hg19 | chr12 | 121,403,462 | 121,417,516 | 14,055 |
| ENST00000701238.1 | hg19 | chr12 | 121,403,462 | 121,418,771 | 15,310 |
| ENST00000646404.1 | hg19 | chr12 | 121,403,463 | 121,417,550 | 14,088 |
| ENST00000537361.1 | hg19 | chr12 | 121,406,416 | 121,418,709 | 12,294 |
| ENST00000433033.3 | hg19 | chr12 | 121,407,827 | 121,417,550 | 9,724 |
| ENST00000535301.2 | hg19 | chr12 | 121,412,178 | 121,418,768 | 6,591 |
Genome browser