NAA38 N-alpha-acetyltransferase 38, NatC auxiliary subunit
Information
- Symbol
- NAA38
- Type
- protein-coding
- Description
- N-alpha-acetyltransferase 38, NatC auxiliary subunit
- Entrez Gene ID
- 84316
- Genome
- hg19
- Position
- chr17:7,760,003-7,761,172
- Genome
- hg38
- Position
- chr17:7,856,685-7,857,854
- MIM
- 617990 OMIM
- HGNC
- HGNC:28212 HGNC
- Ensembl
- ENSG00000183011 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 10 |
Uncertain significance | 0 | 96 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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6 |
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106 |
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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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
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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Category | : |
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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 |
Type | ID |
---|---|
SYNONYM | LSMD1 |
SYNONYM | MAK31 |
SYNONYM | PFAAP2 |
MIM | 617990 OMIM |
HGNC | HGNC:28212 HGNC |
Ensembl | ENSG00000183011 Ensembl |
AllianceGenome | HGNC:28212 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000576384.1 | hg38 | chr17 | 7,856,699 | 7,857,263 | 565 |
ENST00000575071.5 | hg38 | chr17 | 7,856,685 | 7,857,562 | 878 |
ENST00000576861.5 | hg38 | chr17 | 7,856,686 | 7,885,209 | 28,524 |
ENST00000575208.2 | hg38 | chr17 | 7,856,685 | 7,858,079 | 1,395 |
ENST00000333775.9 | hg38 | chr17 | 7,856,685 | 7,857,854 | 1,170 |
ENST00000575771.6 | hg38 | chr17 | 7,856,685 | 7,857,559 | 875 |
ENST00000575771.6 | hg19 | chr17 | 7,760,003 | 7,760,877 | 875 |
ENST00000575071.5 | hg19 | chr17 | 7,760,003 | 7,760,880 | 878 |
ENST00000333775.9 | hg19 | chr17 | 7,760,003 | 7,761,172 | 1,170 |
ENST00000575208.2 | hg19 | chr17 | 7,760,003 | 7,761,397 | 1,395 |
ENST00000576861.5 | hg19 | chr17 | 7,760,004 | 7,788,527 | 28,524 |
ENST00000576384.1 | hg19 | chr17 | 7,760,017 | 7,760,581 | 565 |
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