ENST00000341809.8 KRT77
Information
- Transcript ID
- ENST00000341809.8
- Genome
- hg19
- Position
- chr12:53,083,410-53,097,308
- Strand
- -
- CDS length
- 1,737
- Amino acid length
- 579
- Gene symbol
- KRT77
- Gene type
- protein-coding
- Gene description
- keratin 77
- Gene Entrez Gene ID
- 374454
Variants
Display target variant
Search Word
Target data | : |
MGeND data only
|
Category | : |
|
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 |
---|---|---|
9 | 53,083,410 | 53,085,223 |
8 | 53,085,722 | 53,085,756 |
7 | 53,086,205 | 53,086,425 |
6 | 53,086,539 | 53,086,664 |
5 | 53,088,410 | 53,088,574 |
4 | 53,089,556 | 53,089,651 |
3 | 53,090,154 | 53,090,214 |
2 | 53,091,466 | 53,091,680 |
1 | 53,096,676 | 53,097,308 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
9 | CDS | 53,084,949 | 53,085,223 |
8 | CDS | 53,085,722 | 53,085,756 |
7 | CDS | 53,086,205 | 53,086,425 |
6 | CDS | 53,086,539 | 53,086,664 |
5 | CDS | 53,088,410 | 53,088,574 |
4 | CDS | 53,089,556 | 53,089,651 |
3 | CDS | 53,090,154 | 53,090,214 |
2 | CDS | 53,091,466 | 53,091,680 |
1 | CDS | 53,096,676 | 53,097,218 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr12 | 52,689,626 | 52,703,524 | Link |
CDS sequence
ATGAGCCACCAATTTAGTTCTCAGTCCGCGTTTAGTTCAATGAGCAGGCGGGTTTATAGTACCAGCTCTTCTGCAGGCTCTGGTGGTGGGAGTCCGGCAGTGGGTTCTGTGTGTTATGCTCGAGGGAGGTGTGGTGGTGGTGGATATGGGATCCATGGAAGGGGGTTTGGCTCTAGGAGCCTCTACAATCTGGGTGGCAGTAGAAGCATCTCCATTAATCTAATGGGGAGGAGCACCAGTGGTTTCTGCCAGGGTGGGGGAGTAGGGGGATTTGGAGGGGGCAGAGGCTTTGGGGTTGGCAGCACCGGGGCTGGTGGCTTTGGAGGAGGTGGTTTTGGGGGTGCTGGATTTGGGACTAGCAATTTTGGGCTTGGGGGCTTTGGTCCTTATTGTCCTCCTGGGGGCATCCAAGAGGTGACCATTAACCAGAGCCTCCTAGAGCCACTTCACCTGGAGGTGGACCCTGAAATTCAGAGGATCAAGACCCAGGAGCGGGAGCAGATTATGGTTCTCAACAACAAGTTTGCCTCCTTCATTGACAAGGTGCGATTCCTGGAGCAGCAGAACCAGGTGCTACAAACAAAATGGGAGTTGCTGCAGCAGGTGAACACCTCAACTGGAACCAACAACCTGGAGCCCCTCTTGGAGAACTACATCGGTGACCTGCGGAGGCAGGTGGATTTGCTCAGTGCGGAGCAGATGCGCCAGAACGCGGAGGTCAGGAGCATGCAGGATGTCGTGGAGGACTACAAGAGCAAGTATGAGGATGAAATCAACAAGAGGACTGGCAGCGAGAATGACTTTGTCGTCCTGAAGAAGGATGTGGATGCTGCTTATGTGAGCAAAGTGGACCTGGAGTCCAGGGTGGACACTCTGACTGGGGAGGTCAATTTCTTGAAATATTTATTTTTGACGGAGCTGTCTCAGGTGCAGACTCACATCAGCGACACCAACGTCATCCTGTCCATGGACAATAACCGTTCCCTGGACCTGGACAGCATCATCGATGCAGTGCGGACCCAGTATGAACTGATTGCACAGAGGAGCAAGGACGAGGCCGAAGCCCTGTACCAGACCAAGTACCAGGAGCTCCAGATCACGGCAGGGAGACATGGAGACGACCTGAAGAACAGCAAGATGGAGATTGCAGAGCTCAACCGCACCGTCCAGAGGCTGCAGGCAGAGATCAGCAACGTGAAGAAGCAGATTGAACAGATGCAGTCACTCATTTCGGATGCTGAGGAGAGAGGCGAGCAGGCCCTCCAGGATGCGTGGCAGAAGCTGCAGGACCTGGAGGAGGCCCTGCAGCAGTCCAAGGAGGAGCTGGCCCGGCTGCTGCGTGACTACCAGGCCATGCTGGGGGTCAAGCTGTCCCTGGATGTGGAGATCGCCACCTACCGCCAGCTGCTGGAGGGCGAGGAGAGCAGGATGTCAGGAGAGCTGCAGAGCCATGTGAGCATCTCCGTGCAGAACAGCCAGGTGAGCGTCAACGGCGGCGCGGGAGGCGGCGGCAGCTACGGCTCAGGAGGCTACGGCGGCGGCAGCGGTGGGGGCTATGGCGGCGGAAGAAGCTACCGCGGAGGCGGGGCACGAGGCAGGAGTGGAGGCGGTTATGGCAGCGGCTGCGGCGGCGGTGGCGGGAGCTACGGAGGGAGCGGCAGAAGCGGCCGCGGATCCTCGCGCGTGCAGATCATCCAGACCTCCACCAACACCTCCCACAGGCGGATCTTGGAGTAG
Amino sequence
MSHQFSSQSAFSSMSRRVYSTSSSAGSGGGSPAVGSVCYARGRCGGGGYGIHGRGFGSRSLYNLGGSRSISINLMGRSTSGFCQGGGVGGFGGGRGFGVGSTGAGGFGGGGFGGAGFGTSNFGLGGFGPYCPPGGIQEVTINQSLLEPLHLEVDPEIQRIKTQEREQIMVLNNKFASFIDKVRFLEQQNQVLQTKWELLQQVNTSTGTNNLEPLLENYIGDLRRQVDLLSAEQMRQNAEVRSMQDVVEDYKSKYEDEINKRTGSENDFVVLKKDVDAAYVSKVDLESRVDTLTGEVNFLKYLFLTELSQVQTHISDTNVILSMDNNRSLDLDSIIDAVRTQYELIAQRSKDEAEALYQTKYQELQITAGRHGDDLKNSKMEIAELNRTVQRLQAEISNVKKQIEQMQSLISDAEERGEQALQDAWQKLQDLEEALQQSKEELARLLRDYQAMLGVKLSLDVEIATYRQLLEGEESRMSGELQSHVSISVQNSQVSVNGGAGGGGSYGSGGYGGGSGGGYGGGRSYRGGGARGRSGGGYGSGCGGGGGSYGGSGRSGRGSSRVQIIQTSTNTSHRRILE*