ELOF1 elongation factor 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 2 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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2 |
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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
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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 |
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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 |
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Target data | : |
MGeND data only
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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 | ELF1 |
MIM | 619818 OMIM |
HGNC | HGNC:28691 HGNC |
Ensembl | ENSG00000130165 Ensembl |
AllianceGenome | HGNC:28691 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000589171.5 | hg38 | chr19 | 11,553,457 | 11,559,145 | 5,689 |
ENST00000590700.5 | hg38 | chr19 | 11,553,591 | 11,559,223 | 5,633 |
ENST00000586120.5 | hg38 | chr19 | 11,553,564 | 11,554,794 | 1,231 |
ENST00000252445.8 | hg38 | chr19 | 11,553,046 | 11,559,230 | 6,185 |
ENST00000586683.5 | hg38 | chr19 | 11,551,147 | 11,559,230 | 8,084 |
ENST00000587806.5 | hg38 | chr19 | 11,553,047 | 11,555,467 | 2,421 |
ENST00000591674.5 | hg38 | chr19 | 11,553,531 | 11,555,715 | 2,185 |
ENST00000591912.1 | hg38 | chr19 | 11,553,628 | 11,555,655 | 2,028 |
ENST00000586683.5 | hg19 | chr19 | 11,661,962 | 11,670,045 | 8,084 |
ENST00000252445.8 | hg19 | chr19 | 11,663,861 | 11,670,045 | 6,185 |
ENST00000587806.5 | hg19 | chr19 | 11,663,862 | 11,666,282 | 2,421 |
ENST00000589171.5 | hg19 | chr19 | 11,664,272 | 11,669,960 | 5,689 |
ENST00000591674.5 | hg19 | chr19 | 11,664,346 | 11,666,530 | 2,185 |
ENST00000586120.5 | hg19 | chr19 | 11,664,379 | 11,665,609 | 1,231 |
ENST00000590700.5 | hg19 | chr19 | 11,664,406 | 11,670,038 | 5,633 |
ENST00000591912.1 | hg19 | chr19 | 11,664,443 | 11,666,470 | 2,028 |
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