ENST00000246646.4 KRT38
Information
- Transcript ID
- ENST00000246646.4
- Genome
- hg19
- Position
- chr17:39,592,406-39,597,235
- Strand
- -
- CDS length
- 1,371
- Amino acid length
- 457
- Gene symbol
- KRT38
- Gene type
- protein-coding
- Gene description
- keratin 38
- Gene Entrez Gene ID
- 8687
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| 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 |
|---|---|---|
| 7 | 39,592,406 | 39,593,793 |
| 6 | 39,594,345 | 39,594,565 |
| 5 | 39,594,743 | 39,594,868 |
| 4 | 39,594,949 | 39,595,110 |
| 3 | 39,595,455 | 39,595,611 |
| 2 | 39,596,413 | 39,596,495 |
| 1 | 39,596,682 | 39,597,235 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 7 | CDS | 39,593,664 | 39,593,793 |
| 6 | CDS | 39,594,345 | 39,594,565 |
| 5 | CDS | 39,594,743 | 39,594,868 |
| 4 | CDS | 39,594,949 | 39,595,110 |
| 3 | CDS | 39,595,455 | 39,595,611 |
| 2 | CDS | 39,596,413 | 39,596,495 |
| 1 | CDS | 39,596,682 | 39,597,173 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr17 | 41,436,154 | 41,440,983 | Link |
CDS sequence
ATGACCTCTTCCTACAGCAGCTCCTCATGCCCTCTGGGTTGCACCATGGCTCCTGGAGCAAGAAATGTCTCTGTCTCTCCCATCGACATTGGGTGCCAGCCTGGGGCAGAGGCCAACATTGCCCCCATGTGCCTTTTGGCCAACGTGGCACATGCCAACCGAGTCCGTGTGGGGTCCACTCCCCTGGGCCGCCCCAGCCTCTGTCTGCCGCCTACCTGCCACACTGCTTGTCCCTTGCCAGGGACCTGCCACATTCCTGGCAACATTGGAATCTGTGGGGCCTATGGTGAAAACACCCTGAATGGCCATGAGAAGGAGACCATGCAGTTCCTGAATGACCGCCTGGCCAACTACCTGGAGAAGGTGCGCCAGCTGGAGCAGGAGAATGCGGAGCTGGAGGCCACACTCCTCGAGAGGAGCAAGTGCCACGAGTCCACCGTGTGCCCCGACTACCAGTCTTACTTCCACACCATCGAGGAGCTCCAACAGAAGATCCTGTGCAGCAAGGCCGAGAATGCCAGGCTGATTGTACAAATTGACAATGCCAAGCTGGCTGCCGATGACTTTAGGATCAAGCTGGAGAGTGAGCGCTCCCTGCGCCAGCTGGTGGAGGCAGACAAGTGTGGGACACAGAAGCTCCTGGATGATGCGACCCTGGCCAAGGCCGACCTGGAGGCCCAGCAGGAGTCCCTGAAGGAGGAGCAGCTCTCCCTCAAGAGCAACCACGAGCAGGAAGTAAAGATTCTGAGGAGTCAGCTGGGGGAGAAGCTCCGGATTGAGCTGGACATTGAGCCCACCATTGACCTGAACAGGGTGCTGGGGGAGATGCGGGCTCAGTATGAGGCCATGTTGGAGACCAACCGCCAGGATGTGGAACAGTGGTTCCAAGCCCAGTCTGAAGGCATCAGCCTGCAGGACATGTCCTGCTCCGAGGAGCTGCAGTGCTGCCAGTCGGAGATCCTGGAGCTGAGATGCACGGTGAATGCCCTGGAGGTGGAGCGCCAAGCCCAGCACACCTTGAAGGACTGTCTGCAGAACTCCCTGTGTGAAGCCGAGGACCGCTTCGGCACGGAGCTGGCCCAGATGCAGAGCCTCATCAGCAACGTGGAGGAGCAGCTGTCTGAGATCCGGGCCGACCTGGAGCGGCAAAACCAGGAGTACCAGGTGCTGCTGGACGTGAAGACCCGGCTGGAGAATGAGATTGCCACGTACCGGAACCTTCTGGAAAGCGAGGACTGCAAACTCCCCTGCAATCCGTGCTCCACGTCTCCCTCCTGCGTGACTGCCCCCTGTGCTCCTCGCCCAAGCTGTGGCCCCTGCACCACCTGTGGGCCCACCTGTGGAGCCAGCACCACCGGAAGCCGATTCTGA
Amino sequence
MTSSYSSSSCPLGCTMAPGARNVSVSPIDIGCQPGAEANIAPMCLLANVAHANRVRVGSTPLGRPSLCLPPTCHTACPLPGTCHIPGNIGICGAYGENTLNGHEKETMQFLNDRLANYLEKVRQLEQENAELEATLLERSKCHESTVCPDYQSYFHTIEELQQKILCSKAENARLIVQIDNAKLAADDFRIKLESERSLRQLVEADKCGTQKLLDDATLAKADLEAQQESLKEEQLSLKSNHEQEVKILRSQLGEKLRIELDIEPTIDLNRVLGEMRAQYEAMLETNRQDVEQWFQAQSEGISLQDMSCSEELQCCQSEILELRCTVNALEVERQAQHTLKDCLQNSLCEAEDRFGTELAQMQSLISNVEEQLSEIRADLERQNQEYQVLLDVKTRLENEIATYRNLLESEDCKLPCNPCSTSPSCVTAPCAPRPSCGPCTTCGPTCGASTTGSRF*