ELAVL1 ELAV like RNA binding protein 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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14 |
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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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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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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 | ELAV1 |
SYNONYM | HUR |
SYNONYM | Hua |
SYNONYM | MelG |
MIM | 603466 OMIM |
HGNC | HGNC:3312 HGNC |
Ensembl | ENSG00000066044 Ensembl |
AllianceGenome | HGNC:3312 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000407627.7 | hg38 | chr19 | 7,958,573 | 8,005,641 | 47,069 |
ENST00000593807.1 | hg38 | chr19 | 7,963,630 | 8,005,659 | 42,030 |
ENST00000596459.5 | hg38 | chr19 | 7,963,159 | 8,002,203 | 39,045 |
ENST00000407627.7 | hg19 | chr19 | 8,023,457 | 8,070,525 | 47,069 |
ENST00000596459.5 | hg19 | chr19 | 8,028,043 | 8,067,087 | 39,045 |
ENST00000593807.1 | hg19 | chr19 | 8,028,514 | 8,070,543 | 42,030 |
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