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See other RALYL CNV Assays ›
Gene Symbol
RALYL
Assay Reference Genome
Location

Chr.8:84755249 on build GRCh38
Cytoband
8q21.2
Assay ID Hs03689079_cn
Size
Availability Made To Order
Catalog # 4400291
Price
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Assay Details

Target Gene Details

Entrez Gene ID:

 138046

Gene Name:

 RALY RNA binding protein-like

Gene Aliases:

 HNRPCL3

Location:

 Chr.8:84182629-84921844 on Build GRCh38

Assay Gene Location:

 Within Intron 8
Gene Symbol Transcript Accession Exon Location Assay Transcript Location Protein ID
RALYL NM_001100391.1 NP_001093861.1
NM_001100392.1 NP_001093862.1
NM_001100393.1 NP_001093863.1
NM_001287243.1 NP_001274172.1
NM_001287244.1 NP_001274173.1
NM_173848.5 NP_776247.3
XM_011517462.2 XP_011515764.1
XM_017013058.1 XP_016868547.1
XM_017013059.1 XP_016868548.1
XM_017013060.1 XP_016868549.1
XM_017013061.1 XP_016868550.1
XM_017013062.1 XP_016868551.1
XM_017013063.1 XP_016868552.1
XM_017013064.1 XP_016868553.1
XM_017013065.1 XP_016868554.1
XM_017013066.1 XP_016868555.1
XM_017013067.1 XP_016868556.1
XM_017013068.1 XP_016868557.1
XM_017013069.1 XP_016868558.1
XM_017013070.1 XP_016868559.1
XM_017013071.1 XP_016868560.1
XM_017013072.1 XP_016868561.1
XM_017013073.1 XP_016868562.1
XM_017013074.1 XP_016868563.1
XM_017013075.1 XP_016868564.1
XM_017013076.1 XP_016868565.1
XM_017013077.1 XP_016868566.1
XM_017013078.1 XP_016868567.1
XM_017013079.1 XP_016868568.1
XM_017013080.1 XP_016868569.1
XM_017013081.1 XP_016868570.1
XM_017013082.1 XP_016868571.1
XM_017013083.1 XP_016868572.1
XM_017013084.1 XP_016868573.1
XM_017013085.1 XP_016868574.1
XM_017013086.1 XP_016868575.1
XM_017013087.1 XP_016868576.1
AF495529.1 AAO85516.1
AF495530.1 AAO85517.1
AK094543.1
AK095026.1
AK095560.1
AK123437.1 BAC85617.1
BC031090.1 AAH31090.1
DN989439.1

Target Copy Number Variation Details

DGV Version:

 Release date: 2016-05-15, GRCh GRCh38
Target
Variation		 Location CNV
Subtype		 Genes
esv2752268 Chr.8:83893110 - 84989630 on Build GRCh38 Gain RALYL
nsv6283 Chr.8:84724503 - 84757498 on Build GRCh38 Insertion RALYL
nsv831376 Chr.8:84665187 - 84814076 on Build GRCh38 Gain RALYL
nsv483126 Chr.8:83687766 - 85887771 on Build GRCh38 Gain+Loss CA13 LOC101929601 C8orf59 E2F5 CA3-AS1 REXO1L2P CA1 CA3 LOC101929627 REXO1L1P LOC102723322 LOC100288562 RALYL LRRCC1 LOC107986879 CA2

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More Information


Additional Information:

For this assay, SNP(s) [rs79203576] 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 Intronic Non-exonic DGV Variation

Gene Ontology Categories:

Process(es)


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