HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20645469_20645470del , CM000663.2:g.20645469_20645470del | GRCh38 |
NC_000001.10:g.20971962_20971963del , CM000663.1:g.20971962_20971963del | GRCh37 |
NC_000001.9:g.20844549_20844550del | NCBI36 |
NG_008164.1:g.17015_17016del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000321556.5:c.960-91_960-90del (PINK1) MANE Select | ENSP00000364204.3:n.960-91_960-90del | |
ENST00000321556.4:c.960-91_960-90del (PINK1) | ENSP00000364204.3:n.960-91_960-90del | |
ENST00000492302.1:n.2048-91_2048-90del (PINK1) | ||
NM_032409.2:c.960-91_960-90del (PINK1) | NP_115785.1:n.960-91_960-90del | |
NR_046507.1:n.3981+116_3981+117del (PINK1-AS) | ||
NM_032409.3:c.960-91_960-90del (PINK1) MANE Select | NP_115785.1:n.960-91_960-90del |