ENST00000696603.2 USP21
Information
- Transcript ID
- ENST00000696603.2
- Genome
- hg19
- Position
- chr1:161,131,473-161,135,513
- Strand
- +
- CDS length
- 1,299
- Amino acid length
- 433
- Gene symbol
- USP21
- Gene type
- protein-coding
- Gene description
- ubiquitin specific peptidase 21
- Gene Entrez Gene ID
- 27005
Variants
Display target variant
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 |
Exon
Exon number | Start | Stop |
---|---|---|
1 | 161,131,473 | 161,131,673 |
2 | 161,131,828 | 161,131,887 |
3 | 161,132,060 | 161,132,180 |
4 | 161,132,405 | 161,132,516 |
5 | 161,132,709 | 161,132,864 |
6 | 161,133,345 | 161,133,409 |
7 | 161,133,668 | 161,133,771 |
8 | 161,133,954 | 161,134,040 |
9 | 161,134,324 | 161,134,402 |
10 | 161,134,625 | 161,134,732 |
11 | 161,134,819 | 161,134,933 |
12 | 161,135,147 | 161,135,513 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
1 | CDS | 161,131,473 | 161,131,673 |
2 | CDS | 161,131,828 | 161,131,887 |
3 | CDS | 161,132,060 | 161,132,180 |
4 | CDS | 161,132,405 | 161,132,516 |
5 | CDS | 161,132,709 | 161,132,864 |
6 | CDS | 161,133,345 | 161,133,409 |
7 | CDS | 161,133,668 | 161,133,771 |
8 | CDS | 161,133,954 | 161,134,040 |
9 | CDS | 161,134,324 | 161,134,402 |
10 | CDS | 161,134,625 | 161,134,732 |
11 | CDS | 161,134,819 | 161,134,933 |
12 | CDS | 161,135,147 | 161,135,237 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr1 | 161,161,683 | 161,165,723 | Link |
CDS sequence
ACGGGGGCAGGAGGGGGTTTTGGGGGCAGAAAGGTGGGAGTGGTGAGCAGCTGGGCAACCATGCCGGTGCTGGGGGAGTTGCCCCAGGAGCTGCAACGTCAGCTAGCTGAGCAGAGGAGTAAGTGGGCAACAGGTGGGACAGCCATGGCTGAGTCCGTGGTACATTCAGCTGTGATGGGCTTACTGCTCATGACCAGTGAGGCTCATCACACACTCCTTCTGGGCTCTGGTCATGTTGGCCTTCGAAACCTGGGAAACACGTGCTTCCTGAATGCTGTGCTGCAGTGTCTGAGCAGCACTCGACCTCTTCGGGACTTCTGTCTGAGAAGGGACTTCCGGCAAGAGGTGCCTGGAGGAGGCCGAGCCCAAGAGCTCACTGAAGCCTTTGCAGATGTGATTGGTGCCCTCTGGCACCCTGACTCCTGCGAAGCTGTGAATCCTACTCGATTCCGAGCTGTCTTCCAGAAATATGTTCCCTCCTTCTCTGGATACAGCCAGCAGGATGCCCAAGAGTTCCTGAAGCTCCTCATGGAGCGGCTACACCTTGAAATCAACCGCCGAGGCCGCCGGGCTCCACCGATACTTGCCAATGGTCCAGTTCCCTCTCCACCCCGCCGAGGAGGGGCTCTGCTAGAAGAACCTGAGTTAAGTGATGATGACCGAGCCAACCTAATGTGGAAACGTTACCTGGAGCGAGAGGACAGCAAGATTGTGGACCTGTTTGTGGGCCAGTTGAAAAGTTGTCTCAAGTGCCAGGCCTGTGGGTATCGCTCCACGACCTTCGAGGTTTTTTGTGACCTGTCCCTGCCCATCCCCAAGAAAGGATTTGCTGGGGGCAAGGTGTCTCTGCGGGATTGTTTCAACCTTTTCACTAAGGAAGAAGAGCTAGAGTCGGAGAATGCCCCAGTGTGTGACCGATGTCGGCAGAAAACTCGAAGTACCAAAAAGTTGACAGTACAAAGATTCCCTCGAATCCTCGTGCTCCATCTGAATCGATTTTCTGCCTCCCGAGGCTCCATCAAAAAAAGTTCAGTAGGTGTAGACTTTCCACTGCAGCGACTGAGCCTAGGGGACTTTGCCAGTGACAAAGCCGGAAGTCCTGTATACCAGCTGTATGCCCTTTGCAACCACTCAGGCAGCGTCCACTATGGCCACTACACAGCCCTGTGCCGGTGCCAGACTGGTTGGCATGTCTACAATGACTCTCGTGTCTCCCCTGTCAGTGAAAACCAGGTGGCATCCAGCGAGGGCTACGTGCTGTTCTACCAACTGATGCAGGAGCCACCCCGGTGCCTGTGA
Amino sequence
TGAGGGFGGRKVGVVSSWATMPVLGELPQELQRQLAEQRSKWATGGTAMAESVVHSAVMGLLLMTSEAHHTLLLGSGHVGLRNLGNTCFLNAVLQCLSSTRPLRDFCLRRDFRQEVPGGGRAQELTEAFADVIGALWHPDSCEAVNPTRFRAVFQKYVPSFSGYSQQDAQEFLKLLMERLHLEINRRGRRAPPILANGPVPSPPRRGGALLEEPELSDDDRANLMWKRYLEREDSKIVDLFVGQLKSCLKCQACGYRSTTFEVFCDLSLPIPKKGFAGGKVSLRDCFNLFTKEEELESENAPVCDRCRQKTRSTKKLTVQRFPRILVLHLNRFSASRGSIKKSSVGVDFPLQRLSLGDFASDKAGSPVYQLYALCNHSGSVHYGHYTALCRCQTGWHVYNDSRVSPVSENQVASSEGYVLFYQLMQEPPRCL*