HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20645502_20645503insC , CM000663.2:g.20645502_20645503insC | GRCh38 |
NC_000001.10:g.20971995_20971996insC , CM000663.1:g.20971995_20971996insC | GRCh37 |
NC_000001.9:g.20844582_20844583insC | NCBI36 |
NG_008164.1:g.17048_17049insC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000321556.5:c.960-58_960-57insC (PINK1) MANE Select | ENSP00000364204.3:n.960-58_960-57insC | |
ENST00000321556.4:c.960-58_960-57insC (PINK1) | ENSP00000364204.3:n.960-58_960-57insC | |
ENST00000492302.1:n.2048-58_2048-57insC (PINK1) | ||
NM_032409.2:c.960-58_960-57insC (PINK1) | NP_115785.1:n.960-58_960-57insC | |
NR_046507.1:n.3981+82_3981+83insG (PINK1-AS) | ||
NM_032409.3:c.960-58_960-57insC (PINK1) MANE Select | NP_115785.1:n.960-58_960-57insC |