ABRACL ABRA C-terminal like
Information
- Symbol
- ABRACL
- Type
- protein-coding
- Description
- ABRA C-terminal like
- Entrez Gene ID
- 58527
- Genome
- hg19
- Position
- chr6:139,349,882-139,364,439
- Genome
- hg38
- Position
- chr6:139,028,745-139,043,302
- HGNC
- HGNC:21230 HGNC
- Ensembl
- ENSG00000146386 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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12 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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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 |
Search Word
Target data | : |
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 |
---|---|
SYNONYM | C6orf115 |
SYNONYM | Costars |
SYNONYM | HSPC280 |
SYNONYM | PRO2013 |
HGNC | HGNC:21230 HGNC |
Ensembl | ENSG00000146386 Ensembl |
AllianceGenome | HGNC:21230 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000461027.1 | hg38 | chr6 | 139,028,842 | 139,034,576 | 5,735 |
ENST00000367660.4 | hg38 | chr6 | 139,028,745 | 139,043,302 | 14,558 |
ENST00000367660.4 | hg19 | chr6 | 139,349,882 | 139,364,439 | 14,558 |
ENST00000461027.1 | hg19 | chr6 | 139,349,979 | 139,355,713 | 5,735 |
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