HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20645504_20645505insGA , CM000663.2:g.20645504_20645505insGA | GRCh38 |
NC_000001.10:g.20971997_20971998insGA , CM000663.1:g.20971997_20971998insGA | GRCh37 |
NC_000001.9:g.20844584_20844585insGA | NCBI36 |
NG_008164.1:g.17050_17051insGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321556.5:c.960-56_960-55insGA (PINK1) MANE Select | ENSP00000364204.3:n.960-56_960-55insGA | |
ENST00000321556.4:c.960-56_960-55insGA (PINK1) | ENSP00000364204.3:n.960-56_960-55insGA | |
ENST00000492302.1:n.2048-56_2048-55insGA (PINK1) | ||
NM_032409.2:c.960-56_960-55insGA (PINK1) | NP_115785.1:n.960-56_960-55insGA | |
NR_046507.1:n.3981+81_3981+82insCT (PINK1-AS) | ||
NM_032409.3:c.960-56_960-55insGA (PINK1) MANE Select | NP_115785.1:n.960-56_960-55insGA |