Product Details

Assay Reference Genome
Location

Chr.11:123061904 on build GRCh38
Cytoband
11q24.1
Species
Homo sapiens
Variation Type
Copy Number

Additional Information

For this assay, SNP(s) [rs75882958] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Target Gene Details

Entrez Gene ID
3312
Gene Symbol
HSPA8
Gene Name
heat shock protein family A (Hsp70) member 8
Gene Aliases
HEL-33, HEL-S-72p, HSC54, HSC70, HSC71, HSP71, HSP73, HSPA10, LAP-1, LAP1, NIP71
Location
Chr.11:123057492-123062366 on build GRCh38
Assay Gene Location
Within Intron 2
Gene Symbol Transcript Accession Exon Location Assay Location Protein ID
HSPA8 NM_006597.5 NP_006588.1
NM_153201.3 NP_694881.1
XM_011542798.1 XP_011541100.1
AB034951.1 BAB18615.1
AF352832.1 AAK17898.1
AK096100.1
AK129885.1
AK222628.1 BAD96348.1
AK222785.1 BAD96505.1
AK300404.1
AK303935.1
AK310467.1
BC016179.1 AAH16179.1
BC016660.1 AAH16660.1
BC019816.2 AAH19816.1
DC312904.1
DC395565.1
EU668349.1
FJ224294.1

Target Copy Number Variation Details

DGV Version
Release date: 2016-05-15, GRCh GRCh38
Target
Variation
Location CNV
Subtype
Genes
nsv1039284 Chr11:122985952 - 123083303 on Build GRCh38 Gain CLMP SNORD14C HSPA8 SNORD14D LOC341056 SNORD14E

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