HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20648434dup , CM000663.2:g.20648434dup | GRCh38 |
NC_000001.10:g.20974927dup , CM000663.1:g.20974927dup | GRCh37 |
NC_000001.9:g.20847514dup | NCBI36 |
NG_008164.1:g.19980dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321556.5:c.1124-71dup (PINK1) MANE Select | ENSP00000364204.3:n.1124-71dup | |
ENST00000321556.4:c.1124-71dup (PINK1) | ENSP00000364204.3:n.1124-71dup | |
ENST00000400490.2:n.217-71dup (PINK1) | ||
ENST00000492302.1:n.2212-71dup (PINK1) | ||
NM_032409.2:c.1124-71dup (PINK1) | NP_115785.1:n.1124-71dup | |
NR_046507.1:n.3760dup (PINK1-AS) | ||
NM_032409.3:c.1124-71dup (PINK1) MANE Select | NP_115785.1:n.1124-71dup |