CSN1S1 casein alpha s1

Information
Symbol
CSN1S1
Type
protein-coding
Description
casein alpha s1
Entrez Gene ID
1446
Genome
hg19
Position
chr4:70,796,786-70,812,292
Genome
hg38
Position
chr4:69,931,068-69,946,574
MIM
115450 OMIM
HGNC
HGNC:2445 HGNC
Ensembl
ENSG00000126545 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 :
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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
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 CASA
SYNONYM CSN1
MIM 115450 OMIM
HGNC HGNC:2445 HGNC
Ensembl ENSG00000126545 Ensembl
AllianceGenome HGNC:2445
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000505782.5 hg38 chr4 69,932,556 69,946,557 14,002
ENST00000507772.5 hg38 chr4 69,932,556 69,946,557 14,002
ENST00000507763.5 hg38 chr4 69,932,545 69,946,251 13,707
ENST00000246891.9 hg38 chr4 69,931,068 69,946,574 15,507
ENST00000246891.9 hg19 chr4 70,796,786 70,812,292 15,507
ENST00000507763.5 hg19 chr4 70,798,263 70,811,969 13,707
ENST00000505782.5 hg19 chr4 70,798,274 70,812,275 14,002
ENST00000507772.5 hg19 chr4 70,798,274 70,812,275 14,002
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