HNRNPA3 heterogeneous nuclear ribonucleoprotein A3
Information
- Symbol
- HNRNPA3
- Type
- protein-coding
- Description
- heterogeneous nuclear ribonucleoprotein A3
- Entrez Gene ID
- 220988
- Genome
- hg19
- Position
- chr2:178,077,522-178,088,687
- Genome
- hg38
- Position
- chr2:177,212,794-177,223,959
- MIM
- 605372 OMIM
- HGNC
- HGNC:24941 HGNC
- Ensembl
- ENSG00000170144 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 2 | 0 |
Uncertain significance | 0 | 6 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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6 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | 2610510D13Rik |
SYNONYM | D10S102 |
SYNONYM | FBRNP |
SYNONYM | HNRPA3 |
MIM | 605372 OMIM |
HGNC | HGNC:24941 HGNC |
Ensembl | ENSG00000170144 Ensembl |
AllianceGenome | HGNC:24941 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000392524.7 | hg38 | chr2 | 177,212,794 | 177,223,959 | 11,166 |
ENST00000677863.1 | hg38 | chr2 | 177,212,724 | 177,223,920 | 11,197 |
ENST00000676736.1 | hg38 | chr2 | 177,212,749 | 177,223,920 | 11,172 |
ENST00000676681.1 | hg38 | chr2 | 177,212,724 | 177,223,920 | 11,197 |
ENST00000678111.1 | hg38 | chr2 | 177,212,724 | 177,223,942 | 11,219 |
ENST00000679328.1 | hg38 | chr2 | 177,213,266 | 177,220,085 | 6,820 |
ENST00000677043.1 | hg38 | chr2 | 177,212,724 | 177,223,898 | 11,175 |
ENST00000435711.5 | hg38 | chr2 | 177,212,772 | 177,219,865 | 7,094 |
ENST00000411529.6 | hg38 | chr2 | 177,212,749 | 177,223,958 | 11,210 |
ENST00000676874.1 | hg38 | chr2 | 177,212,741 | 177,223,942 | 11,202 |
ENST00000392524.7 | hg19 | chr2 | 178,077,522 | 178,088,687 | 11,166 |
ENST00000411529.6 | hg19 | chr2 | 178,077,477 | 178,088,686 | 11,210 |
ENST00000435711.5 | hg19 | chr2 | 178,077,500 | 178,084,593 | 7,094 |
ENST00000676681.1 | hg19 | chr2 | 178,077,452 | 178,088,648 | 11,197 |
ENST00000676736.1 | hg19 | chr2 | 178,077,477 | 178,088,648 | 11,172 |
ENST00000676874.1 | hg19 | chr2 | 178,077,469 | 178,088,670 | 11,202 |
ENST00000677043.1 | hg19 | chr2 | 178,077,452 | 178,088,626 | 11,175 |
ENST00000677863.1 | hg19 | chr2 | 178,077,452 | 178,088,648 | 11,197 |
ENST00000678111.1 | hg19 | chr2 | 178,077,452 | 178,088,670 | 11,219 |
ENST00000679328.1 | hg19 | chr2 | 178,077,994 | 178,084,813 | 6,820 |
Key | Value |
---|---|
strand | + |
start | 178,077,421 |
Gene Symbol | HNRNPA3 |
Entrez GeneId | 220,988 |
Chr Band | 2q31.2 |
end | 178,088,684 |
chr | chr2 |
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