HCCS-DT HCCS divergent transcript

Information
Symbol
HCCS-DT
Type
ncRNA
Description
HCCS divergent transcript
Entrez Gene ID
121847985
Genome
hg19
Position
chrX:11,072,364-11,129,260
Genome
hg38
Position
chrX:11,054,244-11,111,140
HGNC
HGNC:55698 HGNC
Ensembl
ENSG00000234129 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
not provided 7 0
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
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:55698 HGNC
Ensembl ENSG00000234129 Ensembl
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000658066.1 hg38 chrX 10,859,998 11,111,145 251,148
ENST00000669054.1 hg38 chrX 10,847,578 11,111,220 263,643
ENST00000686676.1 hg38 chrX 11,054,244 11,111,140 56,897
ENST00000608576.5 hg38 chrX 10,963,371 11,111,138 147,768
ENST00000669054.1 hg19 chrX 10,865,697 11,129,340 263,644
ENST00000658066.1 hg19 chrX 10,878,118 11,129,265 251,148
ENST00000608576.5 hg19 chrX 10,981,491 11,129,258 147,768
ENST00000686676.1 hg19 chrX 11,072,364 11,129,260 56,897
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