Assay Details
Target Gene Details
Entrez Gene ID: | 311 |
Gene Name: | annexin A11 |
Gene Aliases: |
ANX11, CAP50 |
Location: |
Chr.10:80153953-80205677 on Build GRCh38 |
Assay Gene Location: | Within Exon 21 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ANXA11 | NM_001157.2 | 15 | 2262 | NP_001148.1 |
| NM_001278407.1 | 17 | 2241 | NP_001265336.1 | |
| NM_001278408.1 | 17 | 2849 | NP_001265337.1 | |
| NM_001278409.1 | 17 | 2580 | NP_001265338.1 | |
| NM_145868.1 | 16 | 2311 | NP_665875.1 | |
| NM_145869.1 | 17 | 2507 | NP_665876.1 | |
| XM_005269741.4 | 13 | 2339 | XP_005269798.1 | |
| XM_011539736.2 | 17 | 2790 | XP_011538038.1 | |
| AJ278463.1 | 15 | 2261 | CAB94995.1 | |
| AJ278464.1 | 16 | 2310 | CAB94996.1 | |
| AJ278465.1 | 17 | 2506 | CAB94997.1 | |
| AL357617.1 | 1 | 51 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv551635 | Chr.10:79925268 - 80212630 on Build GRCh38 | Loss |
|
| esv3623946 | Chr.10:80133465 - 80175734 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs76487007] 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.
Set Membership: |
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Genomic Map