ACLY ATP citrate lyase
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 10 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 106 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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100 |
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20 |
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
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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MGeND data only
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | ACL |
SYNONYM | ATPCL |
SYNONYM | CLATP |
MIM | 108728 OMIM |
HGNC | HGNC:115 HGNC |
Ensembl | ENSG00000131473 Ensembl |
AllianceGenome | HGNC:115 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000352035.7 | hg38 | chr17 | 41,866,918 | 41,918,951 | 52,034 |
ENST00000590151.5 | hg38 | chr17 | 41,866,917 | 41,918,962 | 52,046 |
ENST00000537919.5 | hg38 | chr17 | 41,867,456 | 41,918,983 | 51,528 |
ENST00000353196.5 | hg38 | chr17 | 41,866,931 | 41,919,019 | 52,089 |
ENST00000393896.6 | hg38 | chr17 | 41,867,574 | 41,919,022 | 51,449 |
ENST00000590151.5 | hg19 | chr17 | 40,023,170 | 40,075,215 | 52,046 |
ENST00000352035.7 | hg19 | chr17 | 40,023,171 | 40,075,204 | 52,034 |
ENST00000353196.5 | hg19 | chr17 | 40,023,184 | 40,075,272 | 52,089 |
ENST00000537919.5 | hg19 | chr17 | 40,023,709 | 40,075,236 | 51,528 |
ENST00000393896.6 | hg19 | chr17 | 40,023,827 | 40,075,275 | 51,449 |
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