ENST00000306658.8 KRT28
Information
- Transcript ID
- ENST00000306658.8
- Genome
- hg38
- Position
- chr17:40,792,196-40,799,959
- Strand
- -
- CDS length
- 1,395
- Amino acid length
- 465
- Gene symbol
- KRT28
- Gene type
- protein-coding
- Gene description
- keratin 28
- Gene Entrez Gene ID
- 162605
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 |
---|---|---|
8 | 40,792,196 | 40,792,569 |
7 | 40,793,155 | 40,793,210 |
6 | 40,793,829 | 40,794,046 |
5 | 40,796,916 | 40,797,041 |
4 | 40,797,120 | 40,797,281 |
3 | 40,798,235 | 40,798,391 |
2 | 40,798,917 | 40,798,999 |
1 | 40,799,444 | 40,799,959 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
8 | CDS | 40,792,427 | 40,792,569 |
7 | CDS | 40,793,155 | 40,793,210 |
6 | CDS | 40,793,829 | 40,794,046 |
5 | CDS | 40,796,916 | 40,797,041 |
4 | CDS | 40,797,120 | 40,797,281 |
3 | CDS | 40,798,235 | 40,798,391 |
2 | CDS | 40,798,917 | 40,798,999 |
1 | CDS | 40,799,444 | 40,799,893 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr17 | 38,948,448 | 38,956,211 | Link |
CDS sequence
ATGTCTCTCCAATTTTCTAATGGATCCAGGCATGTTTGCTTAAGGTCTGGAGCTGGATCTGTCAGACCCCTCAATGGAGGTGCAGGCTTTGCAGGCAGCAGTGCATGTGGTGGCTCTGTTGCTGGAAGTGAATTTTCCTGTGCCTTGGGAGGGGGCTTGGGCAGTGTTCCTGGTGGGAGCCATGCTGGTGGTGCCCTTGGAAATGCTGCTTGTATTGGCTTTGCTGGAAGCGAAGGGGGACTCCTCTCTGGAAATGAGAAGGTGACCATGCAAAATCTTAATGACCGCTTGGCATCCTACCTGGATAATGTGCGAGCTCTGGAGGAGGCAAATGCTGAATTAGAGAGAAAAATCAAGGGTTGGTATGAAAAATACGGACCTGGATCTTGCCGTGGACTTGATCATGACTATAGCAGATATCACCTAACAATTGAGGATCTTAAGAATAAGATTATCTCCTCCACTACTACTAATGCTAATGTCATTCTGCAGATTGATAATGCCAGACTGGCTGCTGATGATTTCAGGCTAAAGTATGAAAATGAGCTCACCCTTCACCAAAACGTAGAGGCCGACATCAACGGATTACGGCGAGTCCTGGACGAGCTGACGCTCTGCAGGACCGACCAGGAGCTGCAATATGAGTCTCTGAGTGAGGAGATGACATATCTCAAAAAGAACCACGAAGAGGAGATGAAGGCTCTGCAGTGCGCGGCTGGGGGCAACGTGAACGTGGAGATGAACGCGGCCCCGGGGGTAGACCTCGCGGTTTTGTTGAACAACATGCGAGCGGAGTACGAAGCCCTTGCAGAGCAGAACCGCAAGGACGCGGAGGCCTGGTTCAATGAGAAGAGCGCCTCGCTGCAGCAACAGATCTCCCACGACTCAGGCGCAGCCACTTTCGCCCGGAGCCAGCTCACCGAGATGAGGCGCACCCTGCAGACCCTGGAGATCCAGCTGCAGTCCCTGATGGCCACGAAACACTCCCTGGAGTGCTCCTTGACAGAGACCGAGAGCAACTACTGTACGCAGCTGGCGCAGATCCAGGCTCAGATCGGGGCCCTGGAGGAGCAGCTGCACCAGGTCAGAACCGAGACCGAGGGCCAGAAGCTGGAGTATGAGCATCTCCTCGATGTCAAGGTCCACTTGGAAAAAGAAATTGAGACCTACTGCCGCCTGATAGATGGAGATGGAAATTCATGCTCCAAATCAAAGGGCTTTGGATCAGGAAGCCCTGGGAATTCATCTAAAGATTTATCCAAAACCACACTGGTAAAGACAGTGGTTGAAGAGCTAGATCAACGTGGTAAAGTTCTTTCATCAAGGATTCACTCCATTGAAGAAAAGACATCTAAAATGACCAACGGCAAGACAGAACAAAGGGTTCCTTTCTAG
Amino sequence
MSLQFSNGSRHVCLRSGAGSVRPLNGGAGFAGSSACGGSVAGSEFSCALGGGLGSVPGGSHAGGALGNAACIGFAGSEGGLLSGNEKVTMQNLNDRLASYLDNVRALEEANAELERKIKGWYEKYGPGSCRGLDHDYSRYHLTIEDLKNKIISSTTTNANVILQIDNARLAADDFRLKYENELTLHQNVEADINGLRRVLDELTLCRTDQELQYESLSEEMTYLKKNHEEEMKALQCAAGGNVNVEMNAAPGVDLAVLLNNMRAEYEALAEQNRKDAEAWFNEKSASLQQQISHDSGAATFARSQLTEMRRTLQTLEIQLQSLMATKHSLECSLTETESNYCTQLAQIQAQIGALEEQLHQVRTETEGQKLEYEHLLDVKVHLEKEIETYCRLIDGDGNSCSKSKGFGSGSPGNSSKDLSKTTLVKTVVEELDQRGKVLSSRIHSIEEKTSKMTNGKTEQRVPF*