HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20645498_20645499insCAA , CM000663.2:g.20645498_20645499insCAA | GRCh38 |
NC_000001.10:g.20971991_20971992insCAA , CM000663.1:g.20971991_20971992insCAA | GRCh37 |
NC_000001.9:g.20844578_20844579insCAA | NCBI36 |
NG_008164.1:g.17044_17045insCAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321556.5:c.960-62_960-61insCAA (PINK1) MANE Select | ENSP00000364204.3:n.960-62_960-61insCAA | |
ENST00000321556.4:c.960-62_960-61insCAA (PINK1) | ENSP00000364204.3:n.960-62_960-61insCAA | |
ENST00000492302.1:n.2048-62_2048-61insCAA (PINK1) | ||
NM_032409.2:c.960-62_960-61insCAA (PINK1) | NP_115785.1:n.960-62_960-61insCAA | |
NR_046507.1:n.3981+88_3981+89insGTT (PINK1-AS) | ||
NM_032409.3:c.960-62_960-61insCAA (PINK1) MANE Select | NP_115785.1:n.960-62_960-61insCAA |