HNRNPLL heterogeneous nuclear ribonucleoprotein L like
Information
- Symbol
- HNRNPLL
- Type
- protein-coding
- Description
- heterogeneous nuclear ribonucleoprotein L like
- Entrez Gene ID
- 92906
- Genome
- hg19
- Position
- chr2:38,789,111-38,830,070
- Genome
- hg38
- Position
- chr2:38,561,969-38,602,928
- MIM
- 611208 OMIM
- HGNC
- HGNC:25127 HGNC
- Ensembl
- ENSG00000143889 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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32 |
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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 |
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 |
---|---|
SYNONYM | HNRPLL |
SYNONYM | SRRF |
MIM | 611208 OMIM |
HGNC | HGNC:25127 HGNC |
Ensembl | ENSG00000143889 Ensembl |
AllianceGenome | HGNC:25127 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000378915.7 | hg38 | chr2 | 38,563,186 | 38,602,626 | 39,441 |
ENST00000608859.5 | hg38 | chr2 | 38,563,186 | 38,603,036 | 39,851 |
ENST00000409636.5 | hg38 | chr2 | 38,561,978 | 38,603,029 | 41,052 |
ENST00000410076.5 | hg38 | chr2 | 38,581,075 | 38,602,929 | 21,855 |
ENST00000358367.8 | hg38 | chr2 | 38,563,186 | 38,603,036 | 39,851 |
ENST00000409328.5 | hg38 | chr2 | 38,564,032 | 38,602,857 | 38,826 |
ENST00000449105.8 | hg38 | chr2 | 38,561,969 | 38,602,928 | 40,960 |
ENST00000449105.8 | hg19 | chr2 | 38,789,111 | 38,830,070 | 40,960 |
ENST00000409636.5 | hg19 | chr2 | 38,789,120 | 38,830,171 | 41,052 |
ENST00000378915.7 | hg19 | chr2 | 38,790,328 | 38,829,768 | 39,441 |
ENST00000358367.8 | hg19 | chr2 | 38,790,328 | 38,830,178 | 39,851 |
ENST00000608859.5 | hg19 | chr2 | 38,790,328 | 38,830,178 | 39,851 |
ENST00000409328.5 | hg19 | chr2 | 38,791,174 | 38,829,999 | 38,826 |
ENST00000410076.5 | hg19 | chr2 | 38,808,217 | 38,830,071 | 21,855 |
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