HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20645494_20645495insGAA , CM000663.2:g.20645494_20645495insGAA | GRCh38 |
NC_000001.10:g.20971987_20971988insGAA , CM000663.1:g.20971987_20971988insGAA | GRCh37 |
NC_000001.9:g.20844574_20844575insGAA | NCBI36 |
NG_008164.1:g.17040_17041insGAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321556.5:c.960-66_960-65insGAA (PINK1) MANE Select | ENSP00000364204.3:n.960-66_960-65insGAA | |
ENST00000321556.4:c.960-66_960-65insGAA (PINK1) | ENSP00000364204.3:n.960-66_960-65insGAA | |
ENST00000492302.1:n.2048-66_2048-65insGAA (PINK1) | ||
NM_032409.2:c.960-66_960-65insGAA (PINK1) | NP_115785.1:n.960-66_960-65insGAA | |
NR_046507.1:n.3981+92_3981+93insCTT (PINK1-AS) | ||
NM_032409.3:c.960-66_960-65insGAA (PINK1) MANE Select | NP_115785.1:n.960-66_960-65insGAA |