ENST00000294129.7 NCKIPSD
Information
- Transcript ID
- ENST00000294129.7
- Genome
- hg38
- Position
- chr3:48,673,844-48,685,915
- Strand
- -
- CDS length
- 2,169
- Amino acid length
- 723
- Gene symbol
- NCKIPSD
- Gene type
- protein-coding
- Gene description
- NCK interacting protein with SH3 domain
- Gene Entrez Gene ID
- 51517
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 |
|---|---|---|
| 13 | 48,673,844 | 48,674,747 |
| 12 | 48,678,564 | 48,678,736 |
| 11 | 48,678,877 | 48,678,969 |
| 10 | 48,679,055 | 48,679,183 |
| 9 | 48,679,377 | 48,679,457 |
| 8 | 48,679,575 | 48,679,713 |
| 7 | 48,679,801 | 48,679,887 |
| 6 | 48,680,059 | 48,680,229 |
| 5 | 48,681,287 | 48,681,780 |
| 4 | 48,682,045 | 48,682,156 |
| 3 | 48,682,348 | 48,682,552 |
| 2 | 48,682,903 | 48,683,012 |
| 1 | 48,685,637 | 48,685,915 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 13 | CDS | 48,674,544 | 48,674,747 |
| 12 | CDS | 48,678,564 | 48,678,736 |
| 11 | CDS | 48,678,877 | 48,678,969 |
| 10 | CDS | 48,679,055 | 48,679,183 |
| 9 | CDS | 48,679,377 | 48,679,457 |
| 8 | CDS | 48,679,575 | 48,679,713 |
| 7 | CDS | 48,679,801 | 48,679,887 |
| 6 | CDS | 48,680,059 | 48,680,229 |
| 5 | CDS | 48,681,287 | 48,681,780 |
| 4 | CDS | 48,682,045 | 48,682,156 |
| 3 | CDS | 48,682,348 | 48,682,552 |
| 2 | CDS | 48,682,903 | 48,683,012 |
| 1 | CDS | 48,685,637 | 48,685,807 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr3 | 48,711,277 | 48,723,348 | Link |
CDS sequence
ATGTACCGCGCGCTGTACGCGTTCCGCTCGGCGGAGCCCAACGCGCTGGCGTTCGCCGCGGGCGAGACCTTCCTGGTGCTAGAGCGAAGCAGCGCGCACTGGTGGCTGGCCGCGCGGGCGCGCAGTGGTGAGACGGGCTACGTGCCGCCAGCCTACCTGCGCCGCCTGCAGGGCCTGGAGCAGGATGTCCTCCAGGCCATTGACCGGGCCATCGAGGCTGTACACAACACAGCCATGCGGGATGGTGGCAAGTACAGCCTGGAACAGCGTGGAGTCCTCCAGAAGCTGATCCACCACCGGAAAGAGACCCTGTCACGCAGAGGCCCTTCAGCCTCCAGTGTTGCAGTTATGACCTCATCAACCAGTGACCACCACTTGGATGCTGCTGCAGCCAGGCAGCCCAATGGGGTGTGTCGAGCTGGGTTCGAGCGGCAGCACAGCCTACCCAGTTCTGAGCATCTTGGGGCAGATGGAGGCCTCTACCAGATCCCACTTCCATCTTCCCAGATCCCACCACAGCCTCGCCGAGCAGCACCCACCACACCGCCCCCACCAGTGAAGCGCCGAGACCGCGAGGCCCTGATGGCCTCTGGGAGTGGTGGCCACAACACCATGCCCTCCGGGGGTAACTCTGTGTCCAGCGGCTCCTCAGTCAGCAGCACCTCCCTGGACACGCTCTATACCAGCTCCAGCCCATCTGAACCAGGCTCCAGCTGCTCACCCACACCCCCACCTGTGCCCCGCCGAGGCACCCACACCACCGTGTCCCAAGTCCAGCCCCCTCCCTCCAAGGCATCAGCACCTGAACCCCCTGCAGAAGAAGAAGTGGCAACTGGTACAACCTCAGCCTCTGATGACCTGGAAGCCCTGGGTACACTGAGCCTGGGGACCACAGAGGAGAAGGCAGCAGCTGAGGCGGCTGTGCCCAGGACCATTGGGGCCGAGCTGATGGAGCTGGTGCGGAGAAACACTGGCCTGAGCCACGAATTATGCCGGGTGGCCATCGGCATCATAGTGGGTCACATCCAGGCCTCGGTGCCGGCCAGCTCACCAGTCATGGAGCAGGTCCTCCTCTCACTCGTAGAGGGCAAGGACCTCAGCATGGCCCTGCCCTCAGGGCAGGTCTGCCACGACCAGCAGAGGCTGGAGGTGATCTTTGCAGACCTGGCTCGCCGGAAGGACGACGCCCAGCAGCGCAGTTGGGCACTATATGAGGATGAGGGTGTCATCCGCTGCTACCTAGAGGAGCTGCTGCATATTCTGACTGATGCAGACCCTGAAGTTTGCAAGAAAATGTGCAAGAGAAACGAGTTCGAGTCTGTCCTGGCCTTGGTGGCCTATTACCAAATGGAACACCGAGCATCACTGCGGCTGCTGCTCCTCAAGTGCTTTGGCGCCATGTGCAGCCTGGATGCAGCCATCATCTCCACGCTTGTGTCATCCGTGCTGCCTGTAGAGCTGGCGAGGGACATGCAGACAGACACGCAGGACCACCAGAAACTCTGTTACTCTGCCCTCATCCTGGCCATGGTCTTCTCCATGGGAGAGGCAGTGCCCTATGCACACTATGAGCACCTGGGCACGCCTTTCGCCCAGTTCCTACTGAACATCGTCGAGGATGGGCTGCCCTTGGACACCACAGAGCAGCTGCCGGACCTCTGCGTGAACCTGCTTCTGGCTCTCAACCTGCACCTGCCAGCTGCTGACCAGAATGTCATCATGGCTGCCCTGAGCAAACACGCCAATGTCAAGATCTTCTCCGAGAAGCTGTTGTTGCTCCTGAACAGAGGGGATGACCCTGTGCGCATCTTCAAACATGAGCCACAGCCACCACACTCTGTCCTCAAGTTCCTGCAGGACGTGTTTGGCAGCCCGGCCACAGCTGCCATCTTCTACCACACAGACATGATGGCTCTCATTGACATCACTGTGCGGCACATCGCAGACCTGTCACCAGGAGACAAGCTGCGCATGGAGTACCTCTCCCTGATGCATGCTATAGTCCGCACCACACCCTACCTGCAGCACCGCCACCGGCTACCCGACCTGCAGGCCATACTGCGACGCATCCTGAATGAGGAGGAGACCTCACCCCAGTGCCAGATGGACCGCATGATTGTCCGAGAGATGTGCAAGGAATTCCTGGTGCTGGGGGAGGCTCCCAGCTAG
Amino sequence
MYRALYAFRSAEPNALAFAAGETFLVLERSSAHWWLAARARSGETGYVPPAYLRRLQGLEQDVLQAIDRAIEAVHNTAMRDGGKYSLEQRGVLQKLIHHRKETLSRRGPSASSVAVMTSSTSDHHLDAAAARQPNGVCRAGFERQHSLPSSEHLGADGGLYQIPLPSSQIPPQPRRAAPTTPPPPVKRRDREALMASGSGGHNTMPSGGNSVSSGSSVSSTSLDTLYTSSSPSEPGSSCSPTPPPVPRRGTHTTVSQVQPPPSKASAPEPPAEEEVATGTTSASDDLEALGTLSLGTTEEKAAAEAAVPRTIGAELMELVRRNTGLSHELCRVAIGIIVGHIQASVPASSPVMEQVLLSLVEGKDLSMALPSGQVCHDQQRLEVIFADLARRKDDAQQRSWALYEDEGVIRCYLEELLHILTDADPEVCKKMCKRNEFESVLALVAYYQMEHRASLRLLLLKCFGAMCSLDAAIISTLVSSVLPVELARDMQTDTQDHQKLCYSALILAMVFSMGEAVPYAHYEHLGTPFAQFLLNIVEDGLPLDTTEQLPDLCVNLLLALNLHLPAADQNVIMAALSKHANVKIFSEKLLLLLNRGDDPVRIFKHEPQPPHSVLKFLQDVFGSPATAAIFYHTDMMALIDITVRHIADLSPGDKLRMEYLSLMHAIVRTTPYLQHRHRLPDLQAILRRILNEEETSPQCQMDRMIVREMCKEFLVLGEAPS*