ENST00000305748.7 KRT73
Information
- Transcript ID
- ENST00000305748.7
- Genome
- hg38
- Position
- chr12:52,607,570-52,618,559
- Strand
- -
- CDS length
- 1,623
- Amino acid length
- 541
- Gene symbol
- KRT73
- Gene type
- protein-coding
- Gene description
- keratin 73
- Gene Entrez Gene ID
- 319101
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 |
---|---|---|
9 | 52,607,570 | 52,608,452 |
8 | 52,609,247 | 52,609,281 |
7 | 52,610,615 | 52,610,835 |
6 | 52,611,204 | 52,611,329 |
5 | 52,613,688 | 52,613,852 |
4 | 52,614,579 | 52,614,674 |
3 | 52,615,279 | 52,615,339 |
2 | 52,616,166 | 52,616,380 |
1 | 52,618,078 | 52,618,559 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
9 | CDS | 52,608,196 | 52,608,452 |
8 | CDS | 52,609,247 | 52,609,281 |
7 | CDS | 52,610,615 | 52,610,835 |
6 | CDS | 52,611,204 | 52,611,329 |
5 | CDS | 52,613,688 | 52,613,852 |
4 | CDS | 52,614,579 | 52,614,674 |
3 | CDS | 52,615,279 | 52,615,339 |
2 | CDS | 52,616,166 | 52,616,380 |
1 | CDS | 52,618,078 | 52,618,524 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr12 | 53,001,354 | 53,012,343 | Link |
CDS sequence
ATGAGCCGCCAATTCACCTACAAGTCGGGAGCTGCTGCCAAGGGGGGCTTCAGCGGCTGCTCCGCTGTGCTCTCAGGGGGCAGCTCATCCTCCTACCGAGCAGGGGGCAAAGGGCTCAGTGGAGGCTTCAGCAGTCGGAGCCTTTACAGCCTGGGGGGTGCCCGGAGCATCTCTTTCAATGTGGCCAGTGGCAGTGGGTGGGCAGGAGGCTATGGATTTGGCCGGGGCCGGGCCAGTGGCTTTGCTGGCAGCATGTTTGGCAGTGTGGCCTTGGGGTCCGTGTGTCCGTCGTTGTGCCCGCCCGGGGGTATCCATCAGGTCACCATCAACAAGAGCCTCCTGGCACCCCTGAACGTGGAGCTGGACCCTGAAATCCAGAAAGTGCGTGCCCAGGAGCGGGAGCAGATCAAGGTGCTGAACAACAAGTTCGCCTCCTTCATTGACAAGGTGCGGTTCCTGGAGCAGCAGAACCAGGTGCTGGAGACCAAGTGGGAGCTGCTACAGCAGCTGGACCTGAACAACTGCAAGAATAACCTGGAGCCCATCCTTGAGGGCTACATCAGCAACCTGCGGAAGCAGCTGGAGACGCTGTCTGGGGACAGGGTGAGGCTGGACTCGGAGCTGAGGAGCGTGCGCGAAGTGGTGGAGGACTACAAGAAGAGGTATGAAGAAGAAATAAACAAGCGCACAACTGCTGAGAATGAATTTGTGGTGCTTAAGAAGGACGTGGACGCAGCTTACACGAGCAAAGTGGAGCTGCAGGCCAAGGTGGATGCCCTGGATGGAGAAATCAAGTTCTTCAAGTGTCTGTACGAGGGGGAGACTGCTCAGATCCAGTCCCACATCAGCGACACGTCCATCATCCTGTCCATGGACAACAACCGGAACCTGGACCTGGACAGCATCATTGCTGAGGTCCGTGCCCAGTATGAGGAGATCGCCCGGAAGAGCAAGGCCGAGGCCGAGGCCCTGTACCAGACCAAGTTCCAGGAGCTGCAGCTAGCAGCCGGCCGGCATGGGGATGACCTGAAACACACCAAAAATGAGATCTCAGAGCTGACCCGTCTCATCCAAAGACTGCGCTCGGAGATTGAGAGTGTGAAGAAGCAGTGTGCCAACCTGGAGACGGCCATCGCTGACGCCGAGCAGCGGGGGGACTGTGCCCTCAAGGATGCCAGGGCCAAGCTGGATGAGCTGGAGGGCGCCCTGCAGCAGGCCAAGGAGGAGCTGGCACGGATGCTGCGCGAGTACCAAGAGCTTTTGAGCGTGAAGCTGTCCCTGGATATTGAGATCGCCACCTACCGCAAGCTGCTGGAGGGCGAGGAGTGCAGGATGTCCGGAGAATATACCAACTCCGTGAGCATTTCGGTCATCAACAGCTCCATGGCCGGGATGGCAGGCACAGGGGCTGGCTTTGGATTCAGCAATGCTGGCACCTACGGCTACTGGCCCAGCTCTGTCAGCGGGGGCTACAGCATGCTGCCTGGGGGCTGTGTCACTGGCAGTGGGAACTGTAGCCCCCGTGGGGAAGCCAGGACCAGGCTGGGGAGTGCAAGTGAATTCAGGGACTCCCAGGGAAAGACCTTAGCTCTAAGCTCACCCACCAAAAAAACCATGAGATAA
Amino sequence
MSRQFTYKSGAAAKGGFSGCSAVLSGGSSSSYRAGGKGLSGGFSSRSLYSLGGARSISFNVASGSGWAGGYGFGRGRASGFAGSMFGSVALGSVCPSLCPPGGIHQVTINKSLLAPLNVELDPEIQKVRAQEREQIKVLNNKFASFIDKVRFLEQQNQVLETKWELLQQLDLNNCKNNLEPILEGYISNLRKQLETLSGDRVRLDSELRSVREVVEDYKKRYEEEINKRTTAENEFVVLKKDVDAAYTSKVELQAKVDALDGEIKFFKCLYEGETAQIQSHISDTSIILSMDNNRNLDLDSIIAEVRAQYEEIARKSKAEAEALYQTKFQELQLAAGRHGDDLKHTKNEISELTRLIQRLRSEIESVKKQCANLETAIADAEQRGDCALKDARAKLDELEGALQQAKEELARMLREYQELLSVKLSLDIEIATYRKLLEGEECRMSGEYTNSVSISVINSSMAGMAGTGAGFGFSNAGTYGYWPSSVSGGYSMLPGGCVTGSGNCSPRGEARTRLGSASEFRDSQGKTLALSSPTKKTMR*