NSMCE1-DT NSMCE1 divergent transcript

Information
Symbol
NSMCE1-DT
Type
ncRNA
Description
NSMCE1 divergent transcript
Entrez Gene ID
400512
Genome
hg19
Position
chr16:27,280,190-27,283,297
Genome
hg38
Position
chr16:27,268,869-27,271,976
HGNC
HGNC:51368 HGNC
Ensembl
ENSG00000245888 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:51368 HGNC
Ensembl ENSG00000245888 Ensembl
AllianceGenome HGNC:51368
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000499939.2 hg38 chr16 27,268,869 27,271,976 3,108
ENST00000565060.1 hg38 chr16 27,268,846 27,284,654 15,809
ENST00000566854.5 hg38 chr16 27,268,205 27,290,468 22,264
ENST00000566854.5 hg19 chr16 27,279,526 27,301,789 22,264
ENST00000565060.1 hg19 chr16 27,280,167 27,295,975 15,809
ENST00000499939.2 hg19 chr16 27,280,190 27,283,297 3,108
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