HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20645474_20645475del , CM000663.2:g.20645474_20645475del | GRCh38 |
NC_000001.10:g.20971967_20971968del , CM000663.1:g.20971967_20971968del | GRCh37 |
NC_000001.9:g.20844554_20844555del | NCBI36 |
NG_008164.1:g.17020_17021del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000321556.5:c.960-86_960-85del (PINK1) MANE Select | ENSP00000364204.3:n.960-86_960-85del | |
ENST00000321556.4:c.960-86_960-85del (PINK1) | ENSP00000364204.3:n.960-86_960-85del | |
ENST00000492302.1:n.2048-86_2048-85del (PINK1) | ||
NM_032409.2:c.960-86_960-85del (PINK1) | NP_115785.1:n.960-86_960-85del | |
NR_046507.1:n.3981+111_3981+112del (PINK1-AS) | ||
NM_032409.3:c.960-86_960-85del (PINK1) MANE Select | NP_115785.1:n.960-86_960-85del |