NTRAS non-coding transcript regulating alternative splicing
Information
- Symbol
- NTRAS
- Type
- ncRNA
- Description
- non-coding transcript regulating alternative splicing
- Entrez Gene ID
- 105748977
- Genome
- hg19
- Position
- chr1:211,813,026-211,827,963
- Genome
- hg38
- Position
- chr1:211,639,684-211,654,621
- HGNC
- HGNC:52478 HGNC
- Ensembl
- ENSG00000227764 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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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
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| 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
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| 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
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| Category | : |
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| 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 | LINC01693 |
| HGNC | HGNC:52478 HGNC |
| Ensembl | ENSG00000227764 Ensembl |
| AllianceGenome | HGNC:52478 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000667263.1 | hg38 | chr1 | 211,639,684 | 211,654,621 | 14,938 |
| ENST00000666922.1 | hg38 | chr1 | 211,639,693 | 211,654,603 | 14,911 |
| ENST00000654864.1 | hg38 | chr1 | 211,639,804 | 211,654,622 | 14,819 |
| ENST00000430123.2 | hg38 | chr1 | 211,639,682 | 211,654,624 | 14,943 |
| ENST00000664125.1 | hg38 | chr1 | 211,639,669 | 211,654,625 | 14,957 |
| ENST00000664125.1 | hg19 | chr1 | 211,813,011 | 211,827,967 | 14,957 |
| ENST00000430123.2 | hg19 | chr1 | 211,813,024 | 211,827,966 | 14,943 |
| ENST00000667263.1 | hg19 | chr1 | 211,813,026 | 211,827,963 | 14,938 |
| ENST00000666922.1 | hg19 | chr1 | 211,813,035 | 211,827,945 | 14,911 |
| ENST00000654864.1 | hg19 | chr1 | 211,813,146 | 211,827,964 | 14,819 |
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