PGLS-DT PGLS divergent transcript

Information
Symbol
PGLS-DT
Type
ncRNA
Description
PGLS divergent transcript
Entrez Gene ID
100507551
Genome
hg19
Position
chr19:17,602,196-17,622,284
Genome
hg38
Position
chr19:17,491,387-17,511,475
HGNC
HGNC:55274 HGNC
Ensembl
ENSG00000269439 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Ranking
ClinVar
0
0
0
0
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 :
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
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
HGNC HGNC:55274 HGNC
Ensembl ENSG00000269439 Ensembl
AllianceGenome HGNC:55274
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000598141.2 hg38 chr19 17,489,800 17,511,492 21,693
ENST00000596643.5 hg38 chr19 17,488,990 17,511,889 22,900
ENST00000595116.2 hg38 chr19 17,503,436 17,511,514 8,079
ENST00000615939.1 hg38 chr19 17,510,100 17,510,850 751
ENST00000655024.1 hg38 chr19 17,491,387 17,511,475 20,089
ENST00000596643.5 hg19 chr19 17,599,799 17,622,698 22,900
ENST00000598141.2 hg19 chr19 17,600,609 17,622,301 21,693
ENST00000655024.1 hg19 chr19 17,602,196 17,622,284 20,089
ENST00000595116.2 hg19 chr19 17,614,245 17,622,323 8,079
ENST00000615939.1 hg19 chr19 17,620,909 17,621,659 751
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