AHI1-DT AHI1 divergent transcript
Information
- Symbol
- AHI1-DT
- Type
- ncRNA
- Description
- AHI1 divergent transcript
- Entrez Gene ID
- 100131814
- Genome
- hg19
- Position
- chr6:135,818,930-136,135,128
- Genome
- hg38
- Position
- chr6:135,497,792-135,813,990
- HGNC
- HGNC:32526 HGNC
- Ensembl
- ENSG00000231028 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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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
[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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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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 | C6orf217 |
SYNONYM | LINC00271 |
SYNONYM | NCRNA00271 |
HGNC | HGNC:32526 HGNC |
Ensembl | ENSG00000231028 Ensembl |
AllianceGenome | HGNC:32526 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000666467.1 | hg38 | chr6 | 135,497,831 | 135,690,779 | 192,949 |
ENST00000655302.1 | hg38 | chr6 | 135,497,792 | 135,813,990 | 316,199 |
ENST00000685995.1 | hg38 | chr6 | 135,497,792 | 135,810,937 | 313,146 |
ENST00000664883.1 | hg38 | chr6 | 135,498,429 | 135,649,886 | 151,458 |
ENST00000580741.5 | hg38 | chr6 | 135,497,806 | 135,518,789 | 20,984 |
ENST00000664629.1 | hg38 | chr6 | 135,497,422 | 135,500,438 | 3,017 |
ENST00000702072.1 | hg38 | chr6 | 135,497,854 | 135,828,703 | 330,850 |
ENST00000690910.1 | hg38 | chr6 | 135,497,918 | 135,528,351 | 30,434 |
ENST00000421378.4 | hg38 | chr6 | 135,497,803 | 135,690,838 | 193,036 |
ENST00000438618.2 | hg38 | chr6 | 135,497,969 | 135,642,955 | 144,987 |
ENST00000579057.5 | hg38 | chr6 | 135,497,937 | 135,517,059 | 19,123 |
ENST00000689196.1 | hg38 | chr6 | 135,497,944 | 135,528,351 | 30,408 |
ENST00000438618.2 | hg19 | chr6 | 135,819,107 | 135,964,093 | 144,987 |
ENST00000579057.5 | hg19 | chr6 | 135,819,075 | 135,838,197 | 19,123 |
ENST00000580741.5 | hg19 | chr6 | 135,818,944 | 135,839,927 | 20,984 |
ENST00000664629.1 | hg19 | chr6 | 135,818,560 | 135,821,576 | 3,017 |
ENST00000685995.1 | hg19 | chr6 | 135,818,930 | 136,132,075 | 313,146 |
ENST00000655302.1 | hg19 | chr6 | 135,818,930 | 136,135,128 | 316,199 |
ENST00000421378.4 | hg19 | chr6 | 135,818,941 | 136,011,976 | 193,036 |
ENST00000666467.1 | hg19 | chr6 | 135,818,969 | 136,011,917 | 192,949 |
ENST00000690910.1 | hg19 | chr6 | 135,819,056 | 135,849,489 | 30,434 |
ENST00000702072.1 | hg19 | chr6 | 135,818,992 | 136,149,841 | 330,850 |
ENST00000689196.1 | hg19 | chr6 | 135,819,082 | 135,849,489 | 30,408 |
ENST00000664883.1 | hg19 | chr6 | 135,819,567 | 135,971,024 | 151,458 |
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