ENST00000305748.7 KRT73
Information
- Transcript ID
- ENST00000305748.7
- Genome
- hg19
- Position
- chr12:53,001,354-53,012,343
- 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 | 53,001,354 | 53,002,236 |
8 | 53,003,031 | 53,003,065 |
7 | 53,004,399 | 53,004,619 |
6 | 53,004,988 | 53,005,113 |
5 | 53,007,472 | 53,007,636 |
4 | 53,008,363 | 53,008,458 |
3 | 53,009,063 | 53,009,123 |
2 | 53,009,950 | 53,010,164 |
1 | 53,011,862 | 53,012,343 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
9 | CDS | 53,001,980 | 53,002,236 |
8 | CDS | 53,003,031 | 53,003,065 |
7 | CDS | 53,004,399 | 53,004,619 |
6 | CDS | 53,004,988 | 53,005,113 |
5 | CDS | 53,007,472 | 53,007,636 |
4 | CDS | 53,008,363 | 53,008,458 |
3 | CDS | 53,009,063 | 53,009,123 |
2 | CDS | 53,009,950 | 53,010,164 |
1 | CDS | 53,011,862 | 53,012,308 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr12 | 52,607,570 | 52,618,559 | Link |
CDS sequence
ATGAGCCGCCAATTCACCTACAAGTCGGGAGCTGCTGCCAAGGGGGGCTTCAGCGGCTGCTCCGCTGTGCTCTCAGGGGGCAGCTCATCCTCCTACCGAGCAGGGGGCAAAGGGCTCAGTGGAGGCTTCAGCAGTCGGAGCCTTTACAGCCTGGGGGGTGCCCGGAGCATCTCTTTCAATGTGGCCAGTGGCAGTGGGTGGGCAGGAGGCTATGGATTTGGCCGGGGCCGGGCCAGTGGCTTTGCTGGCAGCATGTTTGGCAGTGTGGCCTTGGGGTCCGTGTGTCCGTCGTTGTGCCCGCCCGGGGGTATCCATCAGGTCACCATCAACAAGAGCCTCCTGGCACCCCTGAACGTGGAGCTGGACCCTGAAATCCAGAAAGTGCGTGCCCAGGAGCGGGAGCAGATCAAGGTGCTGAACAACAAGTTCGCCTCCTTCATTGACAAGGTGCGGTTCCTGGAGCAGCAGAACCAGGTGCTGGAGACCAAGTGGGAGCTGCTACAGCAGCTGGACCTGAACAACTGCAAGAATAACCTGGAGCCCATCCTTGAGGGCTACATCAGCAACCTGCGGAAGCAGCTGGAGACGCTGTCTGGGGACAGGGTGAGGCTGGACTCGGAGCTGAGGAGCGTGCGCGAAGTGGTGGAGGACTACAAGAAGAGGTATGAAGAAGAAATAAACAAGCGCACAACTGCTGAGAATGAATTTGTGGTGCTTAAGAAGGACGTGGACGCAGCTTACACGAGCAAAGTGGAGCTGCAGGCCAAGGTGGATGCCCTGGATGGAGAAATCAAGTTCTTCAAGTGTCTGTACGAGGGGGAGACTGCTCAGATCCAGTCCCACATCAGCGACACGTCCATCATCCTGTCCATGGACAACAACCGGAACCTGGACCTGGACAGCATCATTGCTGAGGTCCGTGCCCAGTATGAGGAGATCGCCCGGAAGAGCAAGGCCGAGGCCGAGGCCCTGTACCAGACCAAGTTCCAGGAGCTGCAGCTAGCAGCCGGCCGGCATGGGGATGACCTGAAACACACCAAAAATGAGATCTCAGAGCTGACCCGTCTCATCCAAAGACTGCGCTCGGAGATTGAGAGTGTGAAGAAGCAGTGTGCCAACCTGGAGACGGCCATCGCTGACGCCGAGCAGCGGGGGGACTGTGCCCTCAAGGATGCCAGGGCCAAGCTGGATGAGCTGGAGGGCGCCCTGCAGCAGGCCAAGGAGGAGCTGGCACGGATGCTGCGCGAGTACCAAGAGCTTTTGAGCGTGAAGCTGTCCCTGGATATTGAGATCGCCACCTACCGCAAGCTGCTGGAGGGCGAGGAGTGCAGGATGTCCGGAGAATATACCAACTCCGTGAGCATTTCGGTCATCAACAGCTCCATGGCCGGGATGGCAGGCACAGGGGCTGGCTTTGGATTCAGCAATGCTGGCACCTACGGCTACTGGCCCAGCTCTGTCAGCGGGGGCTACAGCATGCTGCCTGGGGGCTGTGTCACTGGCAGTGGGAACTGTAGCCCCCGTGGGGAAGCCAGGACCAGGCTGGGGAGTGCAAGTGAATTCAGGGACTCCCAGGGAAAGACCTTAGCTCTAAGCTCACCCACCAAAAAAACCATGAGATAA
Amino sequence
MSRQFTYKSGAAAKGGFSGCSAVLSGGSSSSYRAGGKGLSGGFSSRSLYSLGGARSISFNVASGSGWAGGYGFGRGRASGFAGSMFGSVALGSVCPSLCPPGGIHQVTINKSLLAPLNVELDPEIQKVRAQEREQIKVLNNKFASFIDKVRFLEQQNQVLETKWELLQQLDLNNCKNNLEPILEGYISNLRKQLETLSGDRVRLDSELRSVREVVEDYKKRYEEEINKRTTAENEFVVLKKDVDAAYTSKVELQAKVDALDGEIKFFKCLYEGETAQIQSHISDTSIILSMDNNRNLDLDSIIAEVRAQYEEIARKSKAEAEALYQTKFQELQLAAGRHGDDLKHTKNEISELTRLIQRLRSEIESVKKQCANLETAIADAEQRGDCALKDARAKLDELEGALQQAKEELARMLREYQELLSVKLSLDIEIATYRKLLEGEECRMSGEYTNSVSISVINSSMAGMAGTGAGFGFSNAGTYGYWPSSVSGGYSMLPGGCVTGSGNCSPRGEARTRLGSASEFRDSQGKTLALSSPTKKTMR*