Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.10115277C>A , CM000681.2:g.10115277C>A | GRCh38 |
| NC_000019.9:g.10225953C>A , CM000681.1:g.10225953C>A | GRCh37 |
| NC_000019.8:g.10086953C>A | NCBI36 |
| NG_047007.1:g.8757C>A | |
| NG_051197.1:g.9648G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253108.9:c.948-148G>T (EIF3G) MANE Select | ENSP00000253108.3:n.948-148G>T | |
| ENST00000321826.5:c.*539C>A (P2RY11) MANE Select | ENSP00000323872.4:n.*539C>A | |
| ENST00000253108.8:c.948-148G>T (EIF3G) | ENSP00000253108.3:n.948-148G>T | |
| ENST00000321826.4:c.*539C>A (P2RY11) | ENSP00000323872.4:n.*539C>A | |
| ENST00000590158.1:n.967-148G>T (EIF3G) | ||
| ENST00000593054.5:c.342-148G>T (EIF3G) | ENSP00000467187.1:n.342-148G>T | |
| NM_001040664.2:c.*539C>A (PPAN-P2RY11) | NP_001035754.1:n.*539C>A | |
| NM_001198690.1:c.*1423C>A (PPAN-P2RY11) | NP_001185619.1:n.*1423C>A | |
| NM_002566.4:c.*539C>A (P2RY11) | NP_002557.2:n.*539C>A | |
| NM_003755.3:c.948-148G>T (EIF3G) | NP_003746.2:n.948-148G>T | |
| NM_003755.4:c.948-148G>T (EIF3G) | NP_003746.2:n.948-148G>T | |
| NM_002566.5:c.*539C>A (P2RY11) MANE Select | NP_002557.2:n.*539C>A | |
| NM_003755.5:c.948-148G>T (EIF3G) MANE Select | NP_003746.2:n.948-148G>T | |
| NM_001040664.3:c.*539C>A (PPAN-P2RY11) | NP_001035754.1:n.*539C>A | |
| NM_001198690.2:c.*1423C>A (PPAN-P2RY11) | NP_001185619.1:n.*1423C>A |