Assay Details
Target Gene Details
Entrez Gene ID: | 771 |
Gene Name: | carbonic anhydrase 12 |
Gene Aliases: |
CA-XII, CAXII, HsT18816, T18816 |
Location: |
Chr.15:63321378-63382166 on Build GRCh38 |
Assay Gene Location: | Within Exon 11 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
CA12 | NM_001218.4 | 11 | 2723 | NP_001209.1 |
NM_001293642.1 | 9 | 2510 | NP_001280571.1 | |
NM_206925.2 | 10 | 2690 | NP_996808.1 | |
NR_135511.1 | 10 | 2793 | ||
AF037335.1 | 11 | 2448 | AAC63952.1 | |
AF051882.1 | 11 | 2340 | AAC39789.1 | |
AK096845.1 | 9 | 2246 | ||
BC011691.2 | 10 | 2415 | AAH11691.1 | |
BC023981.1 | 11 | 2463 | AAH23981.1 | |
BU167720.1 | 1 | 143 | ||
BU944741.1 | 1 | 52 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1035441 | Chr.15:62406037 - 63349997 on Build GRCh38 | Gain | LACTB LOC101928955 APH1B RPS27L CA12 TLN2 LOC105370854 MGC15885 RAB8B TPM1 MIR190A |
More Information
Additional Information:
For this assay, SNP(s) [rs77227433] 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 Exonic DGV Variation |