Assay Details
Target Gene Details
Entrez Gene ID: | 23428 |
Gene Name: | solute carrier family 7 member 8 |
Gene Aliases: |
LAT2, LPI-PC1 |
Location: |
Chr.14:23125295-23183660 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC7A8 | NM_001267036.1 | 9 | 2860 | NP_001253965.1 |
NM_001267037.1 | 8 | 2605 | NP_001253966.1 | |
NM_012244.3 | 11 | 3821 | NP_036376.2 | |
NM_182728.2 | 9 | 2759 | NP_877392.1 | |
NR_049767.1 | 7 | 2800 | ||
AB037669.1 | 11 | 3784 | BAB21519.1 | |
AF135830.1 | 7 | 2402 | AAF05697.1 | |
AF171669.1 | 11 | 3298 | AAF20381.1 | |
AK094550.1 | 3 | 2306 | ||
AL365342.1 | 6 | 3153 | ||
AL365344.1 | 5 | 2136 | ||
AL365345.1 | 7 | 2438 | ||
AL365346.1 | 3 | 2024 | ||
AL365347.1 | 2 | 1412 | ||
BC036825.1 | 7 | 2651 | AAH36825.1 | |
BC052250.1 | 11 | 3104 | AAH52250.1 | |
Y18483.1 | 11 | 3805 | CAB40137.1 |
More Information
Additional Information:
For this assay, SNP(s) [rs77497420] 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 non-DGV Variation |