ENST00000416649.6 NCKIPSD
Information
- Transcript ID
- ENST00000416649.6
- Genome
- hg19
- Position
- chr3:48,711,277-48,723,317
- Strand
- -
- CDS length
- 2,148
- Amino acid length
- 716
- 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 | 48,711,277 | 48,712,180 |
| 12 | 48,715,997 | 48,716,169 |
| 11 | 48,716,310 | 48,716,402 |
| 10 | 48,716,488 | 48,716,616 |
| 9 | 48,716,810 | 48,716,890 |
| 8 | 48,717,008 | 48,717,146 |
| 7 | 48,717,234 | 48,717,320 |
| 6 | 48,717,492 | 48,717,662 |
| 5 | 48,718,720 | 48,719,213 |
| 4 | 48,719,478 | 48,719,568 |
| 3 | 48,719,781 | 48,719,985 |
| 2 | 48,720,336 | 48,720,445 |
| 1 | 48,723,070 | 48,723,317 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 13 | CDS | 48,711,977 | 48,712,180 |
| 12 | CDS | 48,715,997 | 48,716,169 |
| 11 | CDS | 48,716,310 | 48,716,402 |
| 10 | CDS | 48,716,488 | 48,716,616 |
| 9 | CDS | 48,716,810 | 48,716,890 |
| 8 | CDS | 48,717,008 | 48,717,146 |
| 7 | CDS | 48,717,234 | 48,717,320 |
| 6 | CDS | 48,717,492 | 48,717,662 |
| 5 | CDS | 48,718,720 | 48,719,213 |
| 4 | CDS | 48,719,478 | 48,719,568 |
| 3 | CDS | 48,719,781 | 48,719,985 |
| 2 | CDS | 48,720,336 | 48,720,445 |
| 1 | CDS | 48,723,070 | 48,723,240 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr3 | 48,673,844 | 48,685,884 | Link |
CDS sequence
ATGTACCGCGCGCTGTACGCGTTCCGCTCGGCGGAGCCCAACGCGCTGGCGTTCGCCGCGGGCGAGACCTTCCTGGTGCTAGAGCGAAGCAGCGCGCACTGGTGGCTGGCCGCGCGGGCGCGCAGTGGTGAGACGGGCTACGTGCCGCCAGCCTACCTGCGCCGCCTGCAGGGCCTGGAGCAGGATGTCCTCCAGGCCATTGACCGGGCCATCGAGGCTGTACACAACACAGCCATGCGGGATGGTGGCAAGTACAGCCTGGAACAGCGTGGAGTCCTCCAGAAGCTGATCCACCACCGGAAAGAGACCCTGTCACGCAGAGGCCCTTCAGCCTCCAGTGTTGCAGTTATGACCTCATCAACCAGTGACCACCACTTGGATGCTGCTGCAGCCAGGCAGCCCAATGGGGTGTGTCGAGCTGGGTTCGAGCGGCAGCACAGCCTACCCAGTTCTGAGCATCTTGGGGCAGATGGAGGCCTCTACCAGATCCCACCACAGCCTCGCCGAGCAGCACCCACCACACCGCCCCCACCAGTGAAGCGCCGAGACCGCGAGGCCCTGATGGCCTCTGGGAGTGGTGGCCACAACACCATGCCCTCCGGGGGTAACTCTGTGTCCAGCGGCTCCTCAGTCAGCAGCACCTCCCTGGACACGCTCTATACCAGCTCCAGCCCATCTGAACCAGGCTCCAGCTGCTCACCCACACCCCCACCTGTGCCCCGCCGAGGCACCCACACCACCGTGTCCCAAGTCCAGCCCCCTCCCTCCAAGGCATCAGCACCTGAACCCCCTGCAGAAGAAGAAGTGGCAACTGGTACAACCTCAGCCTCTGATGACCTGGAAGCCCTGGGTACACTGAGCCTGGGGACCACAGAGGAGAAGGCAGCAGCTGAGGCGGCTGTGCCCAGGACCATTGGGGCCGAGCTGATGGAGCTGGTGCGGAGAAACACTGGCCTGAGCCACGAATTATGCCGGGTGGCCATCGGCATCATAGTGGGTCACATCCAGGCCTCGGTGCCGGCCAGCTCACCAGTCATGGAGCAGGTCCTCCTCTCACTCGTAGAGGGCAAGGACCTCAGCATGGCCCTGCCCTCAGGGCAGGTCTGCCACGACCAGCAGAGGCTGGAGGTGATCTTTGCAGACCTGGCTCGCCGGAAGGACGACGCCCAGCAGCGCAGTTGGGCACTATATGAGGATGAGGGTGTCATCCGCTGCTACCTAGAGGAGCTGCTGCATATTCTGACTGATGCAGACCCTGAAGTTTGCAAGAAAATGTGCAAGAGAAACGAGTTCGAGTCTGTCCTGGCCTTGGTGGCCTATTACCAAATGGAACACCGAGCATCACTGCGGCTGCTGCTCCTCAAGTGCTTTGGCGCCATGTGCAGCCTGGATGCAGCCATCATCTCCACGCTTGTGTCATCCGTGCTGCCTGTAGAGCTGGCGAGGGACATGCAGACAGACACGCAGGACCACCAGAAACTCTGTTACTCTGCCCTCATCCTGGCCATGGTCTTCTCCATGGGAGAGGCAGTGCCCTATGCACACTATGAGCACCTGGGCACGCCTTTCGCCCAGTTCCTACTGAACATCGTCGAGGATGGGCTGCCCTTGGACACCACAGAGCAGCTGCCGGACCTCTGCGTGAACCTGCTTCTGGCTCTCAACCTGCACCTGCCAGCTGCTGACCAGAATGTCATCATGGCTGCCCTGAGCAAACACGCCAATGTCAAGATCTTCTCCGAGAAGCTGTTGTTGCTCCTGAACAGAGGGGATGACCCTGTGCGCATCTTCAAACATGAGCCACAGCCACCACACTCTGTCCTCAAGTTCCTGCAGGACGTGTTTGGCAGCCCGGCCACAGCTGCCATCTTCTACCACACAGACATGATGGCTCTCATTGACATCACTGTGCGGCACATCGCAGACCTGTCACCAGGAGACAAGCTGCGCATGGAGTACCTCTCCCTGATGCATGCTATAGTCCGCACCACACCCTACCTGCAGCACCGCCACCGGCTACCCGACCTGCAGGCCATACTGCGACGCATCCTGAATGAGGAGGAGACCTCACCCCAGTGCCAGATGGACCGCATGATTGTCCGAGAGATGTGCAAGGAATTCCTGGTGCTGGGGGAGGCTCCCAGCTAG
Amino sequence
MYRALYAFRSAEPNALAFAAGETFLVLERSSAHWWLAARARSGETGYVPPAYLRRLQGLEQDVLQAIDRAIEAVHNTAMRDGGKYSLEQRGVLQKLIHHRKETLSRRGPSASSVAVMTSSTSDHHLDAAAARQPNGVCRAGFERQHSLPSSEHLGADGGLYQIPPQPRRAAPTTPPPPVKRRDREALMASGSGGHNTMPSGGNSVSSGSSVSSTSLDTLYTSSSPSEPGSSCSPTPPPVPRRGTHTTVSQVQPPPSKASAPEPPAEEEVATGTTSASDDLEALGTLSLGTTEEKAAAEAAVPRTIGAELMELVRRNTGLSHELCRVAIGIIVGHIQASVPASSPVMEQVLLSLVEGKDLSMALPSGQVCHDQQRLEVIFADLARRKDDAQQRSWALYEDEGVIRCYLEELLHILTDADPEVCKKMCKRNEFESVLALVAYYQMEHRASLRLLLLKCFGAMCSLDAAIISTLVSSVLPVELARDMQTDTQDHQKLCYSALILAMVFSMGEAVPYAHYEHLGTPFAQFLLNIVEDGLPLDTTEQLPDLCVNLLLALNLHLPAADQNVIMAALSKHANVKIFSEKLLLLLNRGDDPVRIFKHEPQPPHSVLKFLQDVFGSPATAAIFYHTDMMALIDITVRHIADLSPGDKLRMEYLSLMHAIVRTTPYLQHRHRLPDLQAILRRILNEEETSPQCQMDRMIVREMCKEFLVLGEAPS*