Assay Details
Target Gene Details
Entrez Gene ID: | 9774 |
Gene Name: | BCL2 associated transcription factor 1 |
Gene Aliases: |
BTF, bK211L9.1 |
Location: |
Chr.6:136256863-136290645 on Build GRCh38 |
Assay Gene Location: | Within Exon 14 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
BCLAF1 | NM_001077440.1 | 12 | 5015 | NP_001070908.1 |
NM_001077441.1 | 13 | 4649 | NP_001070909.1 | |
NM_001301038.1 | 13 | 5162 | NP_001287967.1 | |
NM_014739.2 | 13 | 5168 | NP_055554.1 | |
XM_005267237.3 | 12 | 4957 | XP_005267294.1 | |
XM_017011529.1 | 13 | 4636 | XP_016867018.1 | |
XM_017011530.1 | 12 | 5296 | XP_016867019.1 | |
XM_017011531.1 | 12 | 4432 | XP_016867020.1 | |
XM_017011532.1 | 14 | 5331 | XP_016867021.1 | |
BX537576.1 | 1 | 4368 | ||
BX648431.1 | 5 | 2830 | ||
BX648878.1 | 9 | 3909 | ||
D79986.1 | 13 | 5168 |
More Information
Additional Information:
For this assay, SNP(s) [rs76137729] 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 |