Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.20644651C= , CM000663.2:g.20644651C= | GRCh38 |
| NC_000001.10:g.20971144C= , CM000663.1:g.20971144C= | GRCh37 |
| NC_000001.9:g.20843731C= | NCBI36 |
| NG_008164.1:g.16197C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_032409.3:c.938C= (PINK1) MANE Select | NP_115785.1:p.Thr313= |
| ENST00000321556.5:c.938C= (PINK1) MANE Select | ENSP00000364204.3:p.Thr313= |
| NM_032409.2:c.938C= (PINK1) | NP_115785.1:p.Thr313= |
| NR_046507.1:n.3981+934G= (PINK1-AS) | |
| ENST00000321556.4:c.938C= (PINK1) | ENSP00000364204.3:p.Thr313= |
| ENST00000492302.1:n.2026C= (PINK1) |