ARGLU1-DT ARGLU1 divergent transcript

Information
Symbol
ARGLU1-DT
Type
ncRNA
Description
ARGLU1 divergent transcript
Entrez Gene ID
283483
Genome
hg19
Position
chr13:107,220,831-107,369,027
Genome
hg38
Position
chr13:106,568,483-106,716,679
HGNC
HGNC:43691 HGNC
Ensembl
ENSG00000272274 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
SYNONYM LINC00551
HGNC HGNC:43691 HGNC
Ensembl ENSG00000272274 Ensembl
AllianceGenome HGNC:43691
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000661468.1 hg38 chr13 106,626,647 106,631,659 5,013
ENST00000656762.1 hg38 chr13 106,669,020 106,671,916 2,897
ENST00000665026.1 hg38 chr13 106,568,435 106,622,254 53,820
ENST00000715700.1 hg38 chr13 106,568,267 106,672,177 103,911
ENST00000658356.1 hg38 chr13 106,653,897 106,671,679 17,783
ENST00000663663.1 hg38 chr13 106,568,483 106,716,679 148,197
ENST00000421601.2 hg38 chr13 106,653,916 106,672,163 18,248
ENST00000653952.1 hg38 chr13 106,568,261 106,631,652 63,392
ENST00000700965.1 hg38 chr13 106,568,208 106,589,024 20,817
ENST00000607593.1 hg38 chr13 106,617,810 106,631,359 13,550
ENST00000690745.1 hg38 chr13 106,568,258 106,574,140 5,883
ENST00000700965.1 hg19 chr13 107,220,556 107,241,372 20,817
ENST00000690745.1 hg19 chr13 107,220,606 107,226,488 5,883
ENST00000653952.1 hg19 chr13 107,220,609 107,284,000 63,392
ENST00000715700.1 hg19 chr13 107,220,615 107,324,525 103,911
ENST00000665026.1 hg19 chr13 107,220,783 107,274,602 53,820
ENST00000663663.1 hg19 chr13 107,220,831 107,369,027 148,197
ENST00000607593.1 hg19 chr13 107,270,158 107,283,707 13,550
ENST00000661468.1 hg19 chr13 107,278,995 107,284,007 5,013
ENST00000658356.1 hg19 chr13 107,306,245 107,324,027 17,783
ENST00000421601.2 hg19 chr13 107,306,264 107,324,511 18,248
ENST00000656762.1 hg19 chr13 107,321,368 107,324,264 2,897
Genome browser