LINC01287 long intergenic non-protein coding RNA 1287
Information
- Symbol
- LINC01287
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1287
- Entrez Gene ID
- 103724390
- Genome
- hg19
- Position
- chr7:153,096,594-153,111,019
- Genome
- hg38
- Position
- chr7:153,399,509-153,413,934
- HGNC
- HGNC:50351 HGNC
- Ensembl
- ENSG00000234722 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
Ranking
ClinVar | |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | TCONS_l2_00027522 |
HGNC | HGNC:50351 HGNC |
Ensembl | ENSG00000234722 Ensembl |
AllianceGenome | HGNC:50351 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000669159.1 | hg38 | chr7 | 153,399,919 | 153,413,948 | 14,030 |
ENST00000665005.1 | hg38 | chr7 | 153,400,313 | 153,413,061 | 12,749 |
ENST00000669370.1 | hg38 | chr7 | 153,399,919 | 153,413,934 | 14,016 |
ENST00000647863.1 | hg38 | chr7 | 153,355,365 | 153,413,981 | 58,617 |
ENST00000669109.1 | hg38 | chr7 | 153,399,509 | 153,413,934 | 14,426 |
ENST00000657245.1 | hg38 | chr7 | 153,399,839 | 153,413,985 | 14,147 |
ENST00000663904.1 | hg38 | chr7 | 153,399,921 | 153,412,571 | 12,651 |
ENST00000658825.1 | hg38 | chr7 | 153,400,322 | 153,413,942 | 13,621 |
ENST00000666243.1 | hg38 | chr7 | 153,399,917 | 153,413,936 | 14,020 |
ENST00000647863.1 | hg19 | chr7 | 153,052,450 | 153,111,066 | 58,617 |
ENST00000658825.1 | hg19 | chr7 | 153,097,407 | 153,111,027 | 13,621 |
ENST00000663904.1 | hg19 | chr7 | 153,097,006 | 153,109,656 | 12,651 |
ENST00000666243.1 | hg19 | chr7 | 153,097,002 | 153,111,021 | 14,020 |
ENST00000665005.1 | hg19 | chr7 | 153,097,398 | 153,110,146 | 12,749 |
ENST00000657245.1 | hg19 | chr7 | 153,096,924 | 153,111,070 | 14,147 |
ENST00000669109.1 | hg19 | chr7 | 153,096,594 | 153,111,019 | 14,426 |
ENST00000669159.1 | hg19 | chr7 | 153,097,004 | 153,111,033 | 14,030 |
ENST00000669370.1 | hg19 | chr7 | 153,097,004 | 153,111,019 | 14,016 |
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