ENST00000254963.7 HSPA12B
Information
- Transcript ID
- ENST00000254963.7
- Genome
- hg19
- Position
- chr20:3,713,332-3,733,758
- 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 | 3,713,332 | 3,713,441 |
| 2 | 3,719,305 | 3,719,364 |
| 3 | 3,721,462 | 3,721,559 |
| 4 | 3,722,931 | 3,723,055 |
| 5 | 3,725,549 | 3,725,735 |
| 6 | 3,726,140 | 3,726,244 |
| 7 | 3,726,562 | 3,726,678 |
| 8 | 3,728,864 | 3,729,038 |
| 9 | 3,729,879 | 3,729,965 |
| 10 | 3,730,397 | 3,730,501 |
| 11 | 3,730,616 | 3,730,874 |
| 12 | 3,731,451 | 3,731,554 |
| 13 | 3,732,158 | 3,733,758 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 2 | CDS | 3,719,322 | 3,719,364 |
| 3 | CDS | 3,721,462 | 3,721,559 |
| 4 | CDS | 3,722,931 | 3,723,055 |
| 5 | CDS | 3,725,549 | 3,725,735 |
| 6 | CDS | 3,726,140 | 3,726,244 |
| 7 | CDS | 3,726,562 | 3,726,678 |
| 8 | CDS | 3,728,864 | 3,729,038 |
| 9 | CDS | 3,729,879 | 3,729,965 |
| 10 | CDS | 3,730,397 | 3,730,501 |
| 11 | CDS | 3,730,616 | 3,730,874 |
| 12 | CDS | 3,731,451 | 3,731,554 |
| 13 | CDS | 3,732,158 | 3,732,813 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr20 | 3,732,685 | 3,753,111 | Link |
CDS sequence
ATGTTGGCTGTCCCGGAGATGGGCCTGCAGGGGCTGTACATCGGCTCCAGCCCGGAGCGGTCCCCAGTGCCTAGCCCACCCGGCTCCCCGAGGACCCAGGAAAGCTGCGGCATTGCCCCCCTCACACCCTCGCAGTCTCCAAAACCCGAGGTCCGAGCCCCCCAGCAGGCCTCCTTCTCTGTGGTGGTGGCCATTGACTTCGGCACCACGTCTAGTGGCTATGCTTTCAGCTTTGCCAGTGACCCTGAGGCCATCCACATGATGAGGAAATGGGAGGGCGGAGACCCGGGCGTGGCCCACCAGAAGACCCCGACCTGCCTGCTGCTGACTCCGGAGGGCGCCTTCCACAGCTTTGGCTACACCGCCCGCGATTACTACCATGACCTGGACCCCGAAGAGGCGCGGGACTGGCTCTACTTCGAGAAGTTCAAGATGAAGATCCACAGCGCCACGGATCTCACCTTGAAGACCCAGCTAGAGGCAGTAAATGGAAAGACGATGCCCGCCCTGGAGGTGTTCGCCCATGCCCTGCGCTTCTTCAGGGAGCACGCCCTTCAGGAGCTGAGGGAGCAGAGCCCATCGCTGCCAGAGAAGGACACTGTGCGCTGGGTGTTGACGGTGCCTGCCATCTGGAAACAGCCAGCCAAGCAGTTCATGCGGGAGGCTGCCTACCTGGCTGGACTAGTGTCCCGAGAGAATGCAGAGCAGCTACTCATCGCCCTGGAGCCCGAGGCCGCCTCGGTATACTGCCGCAAGCTGCGCCTGCACCAGCTCCTGGACCTGAGTGGCCGGGCCCCAGGTGGTGGGCGCCTGGGTGAGCGCCGCTCCATCGACTCCAGCTTCCGTCAGGCTCGGGAGCAGCTGCGAAGGTCCCGCCACAGCCGCACGTTCCTGGTGGAGTCAGGCGTAGGAGAGCTGTGGGCAGAGATGCAAGCAGGAGACCGCTACGTGGTGGCCGACTGCGGCGGAGGCACCGTGGACCTGACGGTGCACCAGCTGGAGCAGCCCCATGGCACCCTCAAGGAGCTCTACAAGGCATCTGGGGGCCCTTATGGCGCGGTGGGCGTGGACCTGGCCTTCGAGCAGCTGCTGTGCCGCATCTTCGGCGAGGACTTCATCGCCACCTTCAAAAGGCAACGGCCGGCAGCCTGGGTAGATCTGACCATCGCCTTCGAGGCTCGCAAGCGCACTGCTGGCCCACACCGTGCAGGGGCGCTCAACATCTCGCTGCCCTTCTCCTTCATTGACTTCTACCGCAAGCAGCGGGGCCACAACGTGGAGACCGCTCTGCGCAGGAGCAGCGTGAACTTCGTGAAGTGGTCCTCACAGGGGATGCTCCGAATGTCTTGTGAAGCCATGAACGAGCTCTTTCAGCCCACCGTCAGCGGGATCATCCAGCACATAGAGGCCCTGCTGGCACGGCCGGAGGTGCAGGGTGTGAAGCTGCTGTTCCTAGTGGGCGGCTTCGCCGAGTCAGCGGTGCTGCAGCACGCGGTGCAGGCGGCGCTGGGCGCCCGCGGTCTGCGTGTCGTGGTCCCGCACGACGTGGGCCTCACCATCCTCAAAGGCGCGGTGCTGTTCGGCCAGGCGCCGGGCGTGGTGCGGGTCCGCCGCTCGCCGCTCACCTATGGCGTGGGCGTGCTCAACCGCTTTGTGCCTGGGCGCCACCCGCCCGAAAAGCTGCTGGTTCGCGACGGCCGCCGCTGGTGCACCGACGTCTTCGAGCGCTTCGTGGCCGCCGAGCAGTCGGTGGCCCTGGGCGAGGAGGTGCGGCGCAGCTACTGCCCGGCGCGTCCCGGCCAGCGGCGCGTACTCATCAACCTGTACTGCTGCGCGGCAGAGGATGCGCGCTTCATCACCGACCCCGGCGTGCGCAAATGCGGCGCGCTCAGCCTCGAGCTTGAGCCCGCCGACTGCGGCCAGGACACCGCCGGCGCGCCTCCCGGCCGCCGCGAGATCCGCGCCGCCATGCAGTTTGGCGACACCGAAATTAAGGTCACCGCCGTCGACGTCAGCACCAATCGCTCCGTGCGCGCGTCCATCGACTTTCTTTCCAACTGA
Amino sequence
MLAVPEMGLQGLYIGSSPERSPVPSPPGSPRTQESCGIAPLTPSQSPKPEVRAPQQASFSVVVAIDFGTTSSGYAFSFASDPEAIHMMRKWEGGDPGVAHQKTPTCLLLTPEGAFHSFGYTARDYYHDLDPEEARDWLYFEKFKMKIHSATDLTLKTQLEAVNGKTMPALEVFAHALRFFREHALQELREQSPSLPEKDTVRWVLTVPAIWKQPAKQFMREAAYLAGLVSRENAEQLLIALEPEAASVYCRKLRLHQLLDLSGRAPGGGRLGERRSIDSSFRQAREQLRRSRHSRTFLVESGVGELWAEMQAGDRYVVADCGGGTVDLTVHQLEQPHGTLKELYKASGGPYGAVGVDLAFEQLLCRIFGEDFIATFKRQRPAAWVDLTIAFEARKRTAGPHRAGALNISLPFSFIDFYRKQRGHNVETALRRSSVNFVKWSSQGMLRMSCEAMNELFQPTVSGIIQHIEALLARPEVQGVKLLFLVGGFAESAVLQHAVQAALGARGLRVVVPHDVGLTILKGAVLFGQAPGVVRVRRSPLTYGVGVLNRFVPGRHPPEKLLVRDGRRWCTDVFERFVAAEQSVALGEEVRRSYCPARPGQRRVLINLYCCAAEDARFITDPGVRKCGALSLELEPADCGQDTAGAPPGRREIRAAMQFGDTEIKVTAVDVSTNRSVRASIDFLSN*