ENST00000427391.2 FIRRE

Information
Transcript ID
ENST00000427391.2
Genome
hg38
Position
chrX:131,702,652-131,830,643
Strand
-
CDS length
0
Amino acid length
0
Gene symbol
FIRRE
Gene type
ncRNA
Gene description
firre intergenic repeating RNA element
Gene Entrez Gene ID
286467
Variants

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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
Entry Origin Type Annotation Entry Origin Annotation
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MGeND data only
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Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
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Target data :
MGeND data only
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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
Exon
Exon number Start Stop
13 131,702,652 131,703,518
12 131,709,498 131,709,556
11 131,711,651 131,711,720
10 131,749,306 131,749,458
9 131,755,598 131,755,746
8 131,756,611 131,756,709
7 131,768,549 131,768,696
6 131,783,887 131,784,039
5 131,794,324 131,794,466
4 131,795,809 131,796,331
3 131,804,972 131,805,037
2 131,825,222 131,825,365
1 131,830,292 131,830,643
Other genome
Genome Chromosome Start End Links
hg19 chrX 130,836,680 130,964,671 Link
CDS sequence
Amino sequence