Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10115381A>T , CM000681.2:g.10115381A>T | GRCh38 |
| NC_000019.9:g.10226057A>T , CM000681.1:g.10226057A>T | GRCh37 |
| NC_000019.8:g.10087057A>T | NCBI36 |
| NG_047007.1:g.8861A>T | |
| NG_051197.1:g.9544T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253108.9:c.947+98T>A (EIF3G) MANE Select | ENSP00000253108.3:n.947+98T>A | |
| ENST00000253108.8:c.947+98T>A (EIF3G) | ENSP00000253108.3:n.947+98T>A | |
| ENST00000590158.1:n.966+98T>A (EIF3G) | ||
| ENST00000593054.5:c.341+98T>A (EIF3G) | ENSP00000467187.1:n.341+98T>A | |
| NM_001040664.2:c.*643A>T (PPAN-P2RY11) | NP_001035754.1:n.*643A>T | |
| NM_001198690.1:c.*1527A>T (PPAN-P2RY11) | NP_001185619.1:n.*1527A>T | |
| NM_002566.4:c.*643A>T (P2RY11) | NP_002557.2:n.*643A>T | |
| NM_003755.3:c.947+98T>A (EIF3G) | NP_003746.2:n.947+98T>A | |
| NM_003755.4:c.947+98T>A (EIF3G) | NP_003746.2:n.947+98T>A | |
| NM_003755.5:c.947+98T>A (EIF3G) MANE Select | NP_003746.2:n.947+98T>A |