HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20645486_20645487insA , CM000663.2:g.20645486_20645487insA | GRCh38 |
NC_000001.10:g.20971979_20971980insA , CM000663.1:g.20971979_20971980insA | GRCh37 |
NC_000001.9:g.20844566_20844567insA | NCBI36 |
NG_008164.1:g.17032_17033insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321556.5:c.960-74_960-73insA (PINK1) MANE Select | ENSP00000364204.3:n.960-74_960-73insA | |
ENST00000321556.4:c.960-74_960-73insA (PINK1) | ENSP00000364204.3:n.960-74_960-73insA | |
ENST00000492302.1:n.2048-74_2048-73insA (PINK1) | ||
NM_032409.2:c.960-74_960-73insA (PINK1) | NP_115785.1:n.960-74_960-73insA | |
NR_046507.1:n.3981+98_3981+99insT (PINK1-AS) | ||
NM_032409.3:c.960-74_960-73insA (PINK1) MANE Select | NP_115785.1:n.960-74_960-73insA |