HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20645500_20645501insCAA , CM000663.2:g.20645500_20645501insCAA | GRCh38 |
NC_000001.10:g.20971993_20971994insCAA , CM000663.1:g.20971993_20971994insCAA | GRCh37 |
NC_000001.9:g.20844580_20844581insCAA | NCBI36 |
NG_008164.1:g.17046_17047insCAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321556.5:c.960-60_960-59insCAA (PINK1) MANE Select | ENSP00000364204.3:n.960-60_960-59insCAA | |
ENST00000321556.4:c.960-60_960-59insCAA (PINK1) | ENSP00000364204.3:n.960-60_960-59insCAA | |
ENST00000492302.1:n.2048-60_2048-59insCAA (PINK1) | ||
NM_032409.2:c.960-60_960-59insCAA (PINK1) | NP_115785.1:n.960-60_960-59insCAA | |
NR_046507.1:n.3981+86_3981+87insGTT (PINK1-AS) | ||
NM_032409.3:c.960-60_960-59insCAA (PINK1) MANE Select | NP_115785.1:n.960-60_960-59insCAA |