HNRNPL heterogeneous nuclear ribonucleoprotein L

Information
Symbol
HNRNPL
Type
protein-coding
Description
heterogeneous nuclear ribonucleoprotein L
Entrez Gene ID
3191
Genome
hg19
Position
chr19:39,327,010-39,340,626
Genome
hg38
Position
chr19:38,836,370-38,849,986
MIM
603083 OMIM
HGNC
HGNC:5045 HGNC
Ensembl
ENSG00000104824 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 10
Likely benign 0 2
Uncertain significance 0 38
Ranking
ClinVar
0
0
0
50
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
Category :
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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
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
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
TypeID
SYNONYM HNRPL
SYNONYM P/OKcl.14
SYNONYM hnRNP-L
MIM 603083 OMIM
HGNC HGNC:5045 HGNC
Ensembl ENSG00000104824 Ensembl
AllianceGenome HGNC:5045
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000221419.10 hg38 chr19 38,836,370 38,849,986 13,617
ENST00000647557.2 hg38 chr19 38,836,370 38,849,986 13,617
ENST00000600873.5 hg38 chr19 38,836,635 38,852,338 15,704
ENST00000221419.10 hg19 chr19 39,327,010 39,340,626 13,617
ENST00000647557.2 hg19 chr19 39,327,010 39,340,626 13,617
ENST00000600873.5 hg19 chr19 39,327,275 39,342,978 15,704
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