C19orf53 chromosome 19 open reading frame 53
Information
- Symbol
- C19orf53
- Type
- protein-coding
- Description
- chromosome 19 open reading frame 53
- Entrez Gene ID
- 28974
- Genome
- hg19
- Position
- chr19:13,885,270-13,889,587
- Genome
- hg38
- Position
- chr19:13,774,456-13,778,773
- MIM
- 620685 OMIM
- HGNC
- HGNC:24991 HGNC
- Ensembl
- ENSG00000104979 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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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Target data | : |
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 |
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SYNONYM | HSPC023 |
SYNONYM | L10K |
SYNONYM | LYDG10 |
MIM | 620685 OMIM |
HGNC | HGNC:24991 HGNC |
Ensembl | ENSG00000104979 Ensembl |
AllianceGenome | HGNC:24991 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000593274.1 | hg38 | chr19 | 13,774,824 | 13,778,462 | 3,639 |
ENST00000588234.6 | hg38 | chr19 | 13,774,456 | 13,778,773 | 4,318 |
ENST00000588234.6 | hg19 | chr19 | 13,885,270 | 13,889,587 | 4,318 |
ENST00000593274.1 | hg19 | chr19 | 13,885,638 | 13,889,276 | 3,639 |
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