HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20645527_20645528del , CM000663.2:g.20645527_20645528del | GRCh38 |
NC_000001.10:g.20972020_20972021del , CM000663.1:g.20972020_20972021del | GRCh37 |
NC_000001.9:g.20844607_20844608del | NCBI36 |
NG_008164.1:g.17073_17074del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321556.5:c.960-33_960-32del (PINK1) MANE Select | ENSP00000364204.3:n.960-33_960-32del | |
ENST00000321556.4:c.960-33_960-32del (PINK1) | ENSP00000364204.3:n.960-33_960-32del | |
ENST00000400490.2:n.20_21del (PINK1) | ||
ENST00000492302.1:n.2048-33_2048-32del (PINK1) | ||
NM_032409.2:c.960-33_960-32del (PINK1) | NP_115785.1:n.960-33_960-32del | |
NR_046507.1:n.3981+61_3981+62del (PINK1-AS) | ||
NM_032409.3:c.960-33_960-32del (PINK1) MANE Select | NP_115785.1:n.960-33_960-32del |