ANKRD40CL ANKRD40 C-terminal like

Information
Symbol
ANKRD40CL
Type
protein-coding
Description
ANKRD40 C-terminal like
Entrez Gene ID
55018
Genome
hg19
Position
chr17:48,838,724-48,844,274
Genome
hg38
Position
chr17:50,761,363-50,766,913
HGNC
HGNC:26080 HGNC
Ensembl
ENSG00000167117 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
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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 :
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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
TypeID
SYNONYM C17orf73
SYNONYM LINC00483
HGNC HGNC:26080 HGNC
Ensembl ENSG00000167117 Ensembl
AllianceGenome HGNC:26080
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000502517.5 hg38 chr17 50,762,851 50,767,557 4,707
ENST00000643007.1 hg38 chr17 50,761,363 50,766,913 5,551
ENST00000450727.6 hg38 chr17 50,761,030 50,767,518 6,489
ENST00000450727.6 hg19 chr17 48,838,391 48,844,879 6,489
ENST00000643007.1 hg19 chr17 48,838,724 48,844,274 5,551
ENST00000502517.5 hg19 chr17 48,840,212 48,844,918 4,707
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