CAPN14 calpain 14

Information
Symbol
CAPN14
Type
protein-coding
Description
calpain 14
Entrez Gene ID
440854
Genome
hg19
Position
chr2:31,395,922-31,440,381
Genome
hg38
Position
chr2:31,173,056-31,217,515
MIM
610229 OMIM
HGNC
HGNC:16664 HGNC
Ensembl
ENSG00000214711 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 6
Conflicting classifications of pathogenicity 0 2
Uncertain significance 0 104
Ranking
ClinVar
0
0
0
112
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
MIM 610229 OMIM
HGNC HGNC:16664 HGNC
Ensembl ENSG00000214711 Ensembl
AllianceGenome HGNC:16664
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000403897.4 hg38 chr2 31,173,056 31,217,515 44,460
ENST00000403897.4 hg19 chr2 31,395,922 31,440,381 44,460
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