HNRNPA1 heterogeneous nuclear ribonucleoprotein A1
Information
- Symbol
- HNRNPA1
- Type
- protein-coding
- Description
- heterogeneous nuclear ribonucleoprotein A1
- Entrez Gene ID
- 3178
- Genome
- hg19
- Position
- chr12:54,674,510-54,680,871
- Genome
- hg38
- Position
- chr12:54,280,726-54,287,087
- MIM
- 164017 OMIM
- HGNC
- HGNC:5031 HGNC
- Ensembl
- ENSG00000135486 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 1 | 8 |
Likely pathogenic | 0 | 32 |
Benign | 0 | 14 |
Likely benign | 0 | 54 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
![]() |
6 |
![]() |
108 |
![]() |
52 |
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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Search word | : | |
Filtering | : |
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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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
|
Category | : |
|
Search word | : | |
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 | ALS19 |
SYNONYM | ALS20 |
SYNONYM | HNRPA1 |
SYNONYM | HNRPA1L3 |
SYNONYM | IBMPFD3 |
SYNONYM | MPD3 |
SYNONYM | UP 1 |
SYNONYM | hnRNP A1 |
SYNONYM | hnRNP-A1 |
MIM | 164017 OMIM |
HGNC | HGNC:5031 HGNC |
Ensembl | ENSG00000135486 Ensembl |
AllianceGenome | HGNC:5031 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000678077.1 | hg38 | chr12 | 54,280,872 | 54,285,239 | 4,368 |
ENST00000547276.5 | hg38 | chr12 | 54,280,780 | 54,285,251 | 4,472 |
ENST00000340913.11 | hg38 | chr12 | 54,280,726 | 54,287,087 | 6,362 |
ENST00000330752.12 | hg38 | chr12 | 54,280,775 | 54,284,881 | 4,107 |
ENST00000550482.2 | hg38 | chr12 | 54,280,704 | 54,285,842 | 5,139 |
ENST00000677210.1 | hg38 | chr12 | 54,280,663 | 54,285,842 | 5,180 |
ENST00000676794.1 | hg38 | chr12 | 54,280,775 | 54,284,317 | 3,543 |
ENST00000677385.1 | hg38 | chr12 | 54,280,663 | 54,285,843 | 5,181 |
ENST00000546500.5 | hg38 | chr12 | 54,280,193 | 54,287,087 | 6,895 |
ENST00000677249.1 | hg38 | chr12 | 54,280,691 | 54,285,745 | 5,055 |
ENST00000677375.1 | hg38 | chr12 | 54,280,663 | 54,285,229 | 4,567 |
ENST00000546500.5 | hg19 | chr12 | 54,673,977 | 54,680,871 | 6,895 |
ENST00000547276.5 | hg19 | chr12 | 54,674,564 | 54,679,035 | 4,472 |
ENST00000677375.1 | hg19 | chr12 | 54,674,447 | 54,679,013 | 4,567 |
ENST00000677210.1 | hg19 | chr12 | 54,674,447 | 54,679,626 | 5,180 |
ENST00000677385.1 | hg19 | chr12 | 54,674,447 | 54,679,627 | 5,181 |
ENST00000330752.12 | hg19 | chr12 | 54,674,559 | 54,678,665 | 4,107 |
ENST00000676794.1 | hg19 | chr12 | 54,674,559 | 54,678,101 | 3,543 |
ENST00000677249.1 | hg19 | chr12 | 54,674,475 | 54,679,529 | 5,055 |
ENST00000340913.11 | hg19 | chr12 | 54,674,510 | 54,680,871 | 6,362 |
ENST00000550482.2 | hg19 | chr12 | 54,674,488 | 54,679,626 | 5,139 |
ENST00000678077.1 | hg19 | chr12 | 54,674,656 | 54,679,023 | 4,368 |
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