HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31268958_31268959del , CM000668.2:g.31268958_31268959del | GRCh38 |
NC_000006.11:g.31236735_31236736del , CM000668.1:g.31236735_31236736del | GRCh37 |
NC_000006.10:g.31344714_31344715del | NCBI36 |
NG_029422.2:g.8173_8174del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.*210_*211del MANE Select | ENSP00000365402.5:n.*210_*211del | |
ENST00000376228.9:c.*210_*211del | ENSP00000365402.5:n.*210_*211del | |
ENST00000376237.8:c.*898_*899del | ENSP00000365412.4:n.*898_*899del | |
ENST00000383329.7:c.*210_*211del | ENSP00000372819.3:n.*210_*211del | |
ENST00000466892.5:n.544_545del | ||
ENST00000470363.5:n.1069_1070del | ||
ENST00000487245.5:n.1670_1671del | ||
NM_002117.5:c.*210_*211del | NP_002108.4:n.*210_*211del | |
NM_002117.6:c.*210_*211del MANE Select | NP_002108.4:n.*210_*211del |