NME1-NME2 NME1-NME2 readthrough

Information
Symbol
NME1-NME2
Type
protein-coding
Description
NME1-NME2 readthrough
Entrez Gene ID
654364
Genome
hg19
Position
chr17:49,230,997-49,249,103
Genome
hg38
Position
chr17:51,153,636-51,171,742
HGNC
HGNC:33531 HGNC
Ensembl
ENSG00000011052 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 8
Likely benign 0 6
Uncertain significance 0 4
Ranking
ClinVar
0
0
2
14
2
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 NM23-LV
SYNONYM NMELV
HGNC HGNC:33531 HGNC
Ensembl ENSG00000011052 Ensembl
AllianceGenome HGNC:33531
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000393193.6 hg38 chr17 51,153,590 51,171,744 18,155
ENST00000376392.10 hg38 chr17 51,153,604 51,171,744 18,141
ENST00000555572.1 hg38 chr17 51,153,636 51,171,742 18,107
ENST00000393193.6 hg19 chr17 49,230,951 49,249,105 18,155
ENST00000376392.10 hg19 chr17 49,230,965 49,249,105 18,141
ENST00000555572.1 hg19 chr17 49,230,997 49,249,103 18,107
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