ENST00000544106.5 MYNN
Information
- Transcript ID
- ENST00000544106.5
- Genome
- hg38
- Position
- chr3:169,774,265-169,789,716
- Strand
- +
- CDS length
- 1,746
- Amino acid length
- 582
- Gene symbol
- MYNN
- Gene type
- protein-coding
- Gene description
- myoneurin
- Gene Entrez Gene ID
- 55892
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 |
|---|---|---|
| 1 | 169,774,265 | 169,774,561 |
| 2 | 169,778,768 | 169,779,561 |
| 3 | 169,780,590 | 169,780,749 |
| 4 | 169,782,465 | 169,782,643 |
| 5 | 169,783,477 | 169,783,560 |
| 6 | 169,786,416 | 169,789,716 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 169,774,296 | 169,774,561 |
| 2 | CDS | 169,778,768 | 169,779,561 |
| 3 | CDS | 169,780,590 | 169,780,749 |
| 4 | CDS | 169,782,465 | 169,782,643 |
| 5 | CDS | 169,783,477 | 169,783,560 |
| 6 | CDS | 169,786,416 | 169,786,678 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr3 | 169,492,053 | 169,507,504 | Link |
CDS sequence
ATGCAGTATTCGCACCACTGTGAGCACCTTTTAGAGAGACTGAACAAACAGCGGGAAGCAGGTTTTCTCTGTGACTGTACCATAGTGATTGGGGAATTCCAGTTTAAAGCTCATAGGAATGTGCTGGCCTCCTTTAGTGAGTATTTTGGTGCGATCTACAGAAGCACTTCTGAGAACAATGTCTTTCTTGATCAGAGTCAGGTGAAGGCTGATGGATTTCAGAAACTGTTGGAGTTTATATACACAGGAACTTTAAATCTTGACAGTTGGAATGTTAAAGAAATTCATCAGGCTGCTGACTATCTCAAAGTGGAAGAGGTGGTCACTAAATGCAAAATAAAGATGGAAGATTTTGCTTTTATTGCTAATCCTTCTTCTACAGAGATATCTAGTATTACTGGAAACATTGAATTGAATCAACAGACTTGTCTTCTTACTCTGCGAGATTATAATAATCGAGAGAAATCAGAAGTATCTACAGATTTGATTCAGGCAAATCCTAAACAAGGCGCGTTAGCGAAAAAGTCATCTCAAACGAAAAAGAAGAAGAAGGCTTTCAACTCCCCGAAAACAGGGCAGAATAAAACAGTGCAATATCCCAGTGACATCTTAGAGAATGCATCTGTTGAATTATTCCTAGATGCAAATAAACTGCCCACACCTGTAGTAGAACAAGTTGCACAAATAAATGATAATTCAGAACTCGAGTTGACATCAGTTGTGGAAAATACTTTTCCAGCACAAGATATTGTGCACACTGTTACAGTGAAACGGAAACGTGGAAAATCACAGCCAAACTGTGCTCTGAAAGAACACTCTATGTCTAATATAGCCAGCGTCAAGAGTCCTTATGAGGCGGAGAACTCCGGGGAAGAGCTGGATCAGAGGTATTCCAAGGCCAAGCCAATGTGTAACACATGTGGGAAAGTGTTTTCAGAAGCCAGCAGTTTGAGAAGGCACATGAGAATACATAAAGGAGTCAAACCTTACGTCTGCCACTTATGTGGAAAGGCATTTACCCAATGTAACCAGCTGAAAACGCATGTAAGAACTCATACAGGTGAGAAGCCATACAAATGTGAATTGTGTGATAAAGGATTTGCTCAGAAATGTCAGCTAGTCTTCCATAGTCGCATGCATCATGGTGAAGAAAAACCCTATAAATGTGATGTATGCAACTTACAGTTTGCAACTTCTAGCAATCTCAAGATTCATGCAAGGAAGCATAGTGGAGAGAAGCCATATGTCTGTGATAGGTGTGGACAGAGATTTGCTCAAGCCAGCACACTGACCTATCATGTCCGTAGGCATACTGGAGAAAAGCCTTATGTATGTGATACCTGTGGGAAGGCATTTGCTGTCTCTAGTTCTCTTATCACTCATTCTCGAAAACATACAGGTGAAAAACCATACATATGTGGTATTTGTGGGAAAAGTTTTATTTCCTCAGGAGAGCTCAACAAACACTTTCGGTCCCATACAGGTGCAGATAAAACTCTAGACTCCAGTGCAGAGGATCATACTTTGAGTGAACAGGATTCCATACAAAAAAGTCCTTTATCAGAAACTATGGATGTGAAGCCTTCTGATATGACTTTACCATTAGCTCTTCCACTTGGGACTGAGGACCATCACATGCTTCTGCCTGTCACGGATACTCAGTCTCCTACATCAGATACATTGTTGAGGTCAACTGTGAATGGGTATTCAGAACCACAGTTGATTTTTTTACAACAATTATACTGA
Amino sequence
MQYSHHCEHLLERLNKQREAGFLCDCTIVIGEFQFKAHRNVLASFSEYFGAIYRSTSENNVFLDQSQVKADGFQKLLEFIYTGTLNLDSWNVKEIHQAADYLKVEEVVTKCKIKMEDFAFIANPSSTEISSITGNIELNQQTCLLTLRDYNNREKSEVSTDLIQANPKQGALAKKSSQTKKKKKAFNSPKTGQNKTVQYPSDILENASVELFLDANKLPTPVVEQVAQINDNSELELTSVVENTFPAQDIVHTVTVKRKRGKSQPNCALKEHSMSNIASVKSPYEAENSGEELDQRYSKAKPMCNTCGKVFSEASSLRRHMRIHKGVKPYVCHLCGKAFTQCNQLKTHVRTHTGEKPYKCELCDKGFAQKCQLVFHSRMHHGEEKPYKCDVCNLQFATSSNLKIHARKHSGEKPYVCDRCGQRFAQASTLTYHVRRHTGEKPYVCDTCGKAFAVSSSLITHSRKHTGEKPYICGICGKSFISSGELNKHFRSHTGADKTLDSSAEDHTLSEQDSIQKSPLSETMDVKPSDMTLPLALPLGTEDHHMLLPVTDTQSPTSDTLLRSTVNGYSEPQLIFLQQLY*