ARL17A ADP ribosylation factor like GTPase 17A

Information
Symbol
ARL17A
Type
protein-coding
Description
ADP ribosylation factor like GTPase 17A
Entrez Gene ID
51326
Genome
hg19
Position
chr17:44,624,557-44,657,057
Genome
hg38
Position
chr17:46,547,191-46,579,691
HGNC
HGNC:24096 HGNC
Ensembl
ENSG00000185829 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Likely benign 0 30
Uncertain significance 0 110
Ranking
ClinVar
0
0
0
140
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
SYNONYM ARF1P2
SYNONYM ARL17P1
HGNC HGNC:24096 HGNC
Ensembl ENSG00000185829 Ensembl
AllianceGenome HGNC:24096
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000706259.1 hg38 chr17 46,534,622 46,579,685 45,064
ENST00000706258.1 hg38 chr17 46,527,269 46,579,691 52,423
ENST00000706255.1 hg38 chr17 46,516,390 46,579,644 63,255
ENST00000706256.1 hg38 chr17 46,516,697 46,579,671 62,975
ENST00000706253.1 hg38 chr17 46,504,372 46,579,661 75,290
ENST00000706254.1 hg38 chr17 46,507,984 46,579,622 71,639
ENST00000706251.1 hg38 chr17 46,504,367 46,579,691 75,325
ENST00000706260.1 hg38 chr17 46,547,191 46,579,691 32,501
ENST00000622488.6 hg38 chr17 46,528,685 46,579,673 50,989
ENST00000329240.10 hg38 chr17 46,528,740 46,579,671 50,932
ENST00000570550.5 hg38 chr17 46,552,533 46,579,657 27,125
ENST00000336125.6 hg38 chr17 46,552,756 46,579,691 26,936
ENST00000573185.5 hg38 chr17 46,548,207 46,579,651 31,445
ENST00000445552.6 hg38 chr17 46,516,702 46,579,670 62,969
ENST00000706248.1 hg38 chr17 46,503,455 46,579,691 76,237
ENST00000706247.1 hg38 chr17 46,502,443 46,579,671 77,229
ENST00000706245.1 hg38 chr17 46,499,780 46,579,695 79,916
ENST00000706304.1 hg38 chr17 46,508,679 46,579,653 70,975
ENST00000706303.1 hg38 chr17 46,499,806 46,579,661 79,856
ENST00000706245.1 hg19 chr17 44,577,146 44,657,061 79,916
ENST00000706251.1 hg19 chr17 44,581,733 44,657,057 75,325
ENST00000622488.6 hg19 chr17 44,606,051 44,657,039 50,989
ENST00000329240.10 hg19 chr17 44,606,106 44,657,037 50,932
ENST00000706247.1 hg19 chr17 44,579,809 44,657,037 77,229
ENST00000706248.1 hg19 chr17 44,580,821 44,657,057 76,237
ENST00000573185.5 hg19 chr17 44,625,573 44,657,017 31,445
ENST00000570550.5 hg19 chr17 44,629,899 44,657,023 27,125
ENST00000706253.1 hg19 chr17 44,581,738 44,657,027 75,290
ENST00000706254.1 hg19 chr17 44,585,350 44,656,988 71,639
ENST00000706255.1 hg19 chr17 44,593,756 44,657,010 63,255
ENST00000336125.6 hg19 chr17 44,630,122 44,657,057 26,936
ENST00000445552.6 hg19 chr17 44,594,068 44,657,036 62,969
ENST00000706256.1 hg19 chr17 44,594,063 44,657,037 62,975
ENST00000706258.1 hg19 chr17 44,604,635 44,657,057 52,423
ENST00000706259.1 hg19 chr17 44,611,988 44,657,051 45,064
ENST00000706260.1 hg19 chr17 44,624,557 44,657,057 32,501
ENST00000706303.1 hg19 chr17 44,577,172 44,657,027 79,856
ENST00000706304.1 hg19 chr17 44,586,045 44,657,019 70,975
Genome browser