Assay Details
Target Gene Details
Entrez Gene ID: | 6282 |
Gene Name: | S100 calcium binding protein A11 |
Gene Aliases: |
HEL-S-43, MLN70, S100C |
Location: |
Chr.1:152032506-152037035 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 2 - Exon 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
S100A11 | NM_005620.1 | NP_005611.1 | ||
AK312184.1 | ||||
BC001410.2 | AAH01410.1 | |||
BC014354.1 | AAH14354.1 | |||
BT009912.1 | AAP88914.1 | |||
D38583.1 | BAA07597.1 | |||
D49355.1 | BAA08354.1 | |||
D50374.1 | BAA23325.1 | |||
EU794659.1 | ||||
X80201.1 | CAA56492.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1007097 | Chr.1:151860320 - 152255501 on Build GRCh38 | Gain | LOC100131107 TCHH HRNR TCHHL1 THEM4 S100A10 NBPF18P S100A11 RPTN |
More Information
Additional Information:
For this assay, SNP(s) [rs80277426] 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: |
Intragenic Non-exonic DGV Variation |