ENST00000254963.7 HSPA12B
Information
- Transcript ID
- ENST00000254963.7
- Genome
- hg38
- Position
- chr20:3,732,685-3,753,111
- Strand
- +
- CDS length
- 2,061
- Amino acid length
- 687
- Gene symbol
- HSPA12B
- Gene type
- protein-coding
- Gene description
- heat shock protein family A (Hsp70) member 12B
- Gene Entrez Gene ID
- 116835
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 |
|---|---|---|
| 1 | 3,732,685 | 3,732,794 |
| 2 | 3,738,658 | 3,738,717 |
| 3 | 3,740,815 | 3,740,912 |
| 4 | 3,742,284 | 3,742,408 |
| 5 | 3,744,902 | 3,745,088 |
| 6 | 3,745,493 | 3,745,597 |
| 7 | 3,745,915 | 3,746,031 |
| 8 | 3,748,217 | 3,748,391 |
| 9 | 3,749,232 | 3,749,318 |
| 10 | 3,749,750 | 3,749,854 |
| 11 | 3,749,969 | 3,750,227 |
| 12 | 3,750,804 | 3,750,907 |
| 13 | 3,751,511 | 3,753,111 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 2 | CDS | 3,738,675 | 3,738,717 |
| 3 | CDS | 3,740,815 | 3,740,912 |
| 4 | CDS | 3,742,284 | 3,742,408 |
| 5 | CDS | 3,744,902 | 3,745,088 |
| 6 | CDS | 3,745,493 | 3,745,597 |
| 7 | CDS | 3,745,915 | 3,746,031 |
| 8 | CDS | 3,748,217 | 3,748,391 |
| 9 | CDS | 3,749,232 | 3,749,318 |
| 10 | CDS | 3,749,750 | 3,749,854 |
| 11 | CDS | 3,749,969 | 3,750,227 |
| 12 | CDS | 3,750,804 | 3,750,907 |
| 13 | CDS | 3,751,511 | 3,752,166 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr20 | 3,713,332 | 3,733,758 | Link |
CDS sequence
ATGTTGGCTGTCCCGGAGATGGGCCTGCAGGGGCTGTACATCGGCTCCAGCCCGGAGCGGTCCCCAGTGCCTAGCCCACCCGGCTCCCCGAGGACCCAGGAAAGCTGCGGCATTGCCCCCCTCACACCCTCGCAGTCTCCAAAACCCGAGGTCCGAGCCCCCCAGCAGGCCTCCTTCTCTGTGGTGGTGGCCATTGACTTCGGCACCACGTCTAGTGGCTATGCTTTCAGCTTTGCCAGTGACCCTGAGGCCATCCACATGATGAGGAAATGGGAGGGCGGAGACCCGGGCGTGGCCCACCAGAAGACCCCGACCTGCCTGCTGCTGACTCCGGAGGGCGCCTTCCACAGCTTTGGCTACACCGCCCGCGATTACTACCATGACCTGGACCCCGAAGAGGCGCGGGACTGGCTCTACTTCGAGAAGTTCAAGATGAAGATCCACAGCGCCACGGATCTCACCTTGAAGACCCAGCTAGAGGCAGTAAATGGAAAGACGATGCCCGCCCTGGAGGTGTTCGCCCATGCCCTGCGCTTCTTCAGGGAGCACGCCCTTCAGGAGCTGAGGGAGCAGAGCCCATCGCTGCCAGAGAAGGACACTGTGCGCTGGGTGTTGACGGTGCCTGCCATCTGGAAACAGCCAGCCAAGCAGTTCATGCGGGAGGCTGCCTACCTGGCTGGACTAGTGTCCCGAGAGAATGCAGAGCAGCTACTCATCGCCCTGGAGCCCGAGGCCGCCTCGGTATACTGCCGCAAGCTGCGCCTGCACCAGCTCCTGGACCTGAGTGGCCGGGCCCCAGGTGGTGGGCGCCTGGGTGAGCGCCGCTCCATCGACTCCAGCTTCCGTCAGGCTCGGGAGCAGCTGCGAAGGTCCCGCCACAGCCGCACGTTCCTGGTGGAGTCAGGCGTAGGAGAGCTGTGGGCAGAGATGCAAGCAGGAGACCGCTACGTGGTGGCCGACTGCGGCGGAGGCACCGTGGACCTGACGGTGCACCAGCTGGAGCAGCCCCATGGCACCCTCAAGGAGCTCTACAAGGCATCTGGGGGCCCTTATGGCGCGGTGGGCGTGGACCTGGCCTTCGAGCAGCTGCTGTGCCGCATCTTCGGCGAGGACTTCATCGCCACCTTCAAAAGGCAACGGCCGGCAGCCTGGGTAGATCTGACCATCGCCTTCGAGGCTCGCAAGCGCACTGCTGGCCCACACCGTGCAGGGGCGCTCAACATCTCGCTGCCCTTCTCCTTCATTGACTTCTACCGCAAGCAGCGGGGCCACAACGTGGAGACCGCTCTGCGCAGGAGCAGCGTGAACTTCGTGAAGTGGTCCTCACAGGGGATGCTCCGAATGTCTTGTGAAGCCATGAACGAGCTCTTTCAGCCCACCGTCAGCGGGATCATCCAGCACATAGAGGCCCTGCTGGCACGGCCGGAGGTGCAGGGTGTGAAGCTGCTGTTCCTAGTGGGCGGCTTCGCCGAGTCAGCGGTGCTGCAGCACGCGGTGCAGGCGGCGCTGGGCGCCCGCGGTCTGCGTGTCGTGGTCCCGCACGACGTGGGCCTCACCATCCTCAAAGGCGCGGTGCTGTTCGGCCAGGCGCCGGGCGTGGTGCGGGTCCGCCGCTCGCCGCTCACCTATGGCGTGGGCGTGCTCAACCGCTTTGTGCCTGGGCGCCACCCGCCCGAAAAGCTGCTGGTTCGCGACGGCCGCCGCTGGTGCACCGACGTCTTCGAGCGCTTCGTGGCCGCCGAGCAGTCGGTGGCCCTGGGCGAGGAGGTGCGGCGCAGCTACTGCCCGGCGCGTCCCGGCCAGCGGCGCGTACTCATCAACCTGTACTGCTGCGCGGCAGAGGATGCGCGCTTCATCACCGACCCCGGCGTGCGCAAATGCGGCGCGCTCAGCCTCGAGCTTGAGCCCGCCGACTGCGGCCAGGACACCGCCGGCGCGCCTCCCGGCCGCCGCGAGATCCGCGCCGCCATGCAGTTTGGCGACACCGAAATTAAGGTCACCGCCGTCGACGTCAGCACCAATCGCTCCGTGCGCGCGTCCATCGACTTTCTTTCCAACTGA
Amino sequence
MLAVPEMGLQGLYIGSSPERSPVPSPPGSPRTQESCGIAPLTPSQSPKPEVRAPQQASFSVVVAIDFGTTSSGYAFSFASDPEAIHMMRKWEGGDPGVAHQKTPTCLLLTPEGAFHSFGYTARDYYHDLDPEEARDWLYFEKFKMKIHSATDLTLKTQLEAVNGKTMPALEVFAHALRFFREHALQELREQSPSLPEKDTVRWVLTVPAIWKQPAKQFMREAAYLAGLVSRENAEQLLIALEPEAASVYCRKLRLHQLLDLSGRAPGGGRLGERRSIDSSFRQAREQLRRSRHSRTFLVESGVGELWAEMQAGDRYVVADCGGGTVDLTVHQLEQPHGTLKELYKASGGPYGAVGVDLAFEQLLCRIFGEDFIATFKRQRPAAWVDLTIAFEARKRTAGPHRAGALNISLPFSFIDFYRKQRGHNVETALRRSSVNFVKWSSQGMLRMSCEAMNELFQPTVSGIIQHIEALLARPEVQGVKLLFLVGGFAESAVLQHAVQAALGARGLRVVVPHDVGLTILKGAVLFGQAPGVVRVRRSPLTYGVGVLNRFVPGRHPPEKLLVRDGRRWCTDVFERFVAAEQSVALGEEVRRSYCPARPGQRRVLINLYCCAAEDARFITDPGVRKCGALSLELEPADCGQDTAGAPPGRREIRAAMQFGDTEIKVTAVDVSTNRSVRASIDFLSN*