HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20188843_20188844insT , CM000675.2:g.20188843_20188844insT | GRCh38 |
NC_000013.10:g.20762982_20762983insT , CM000675.1:g.20762982_20762983insT | GRCh37 |
NC_000013.9:g.19660982_19660983insT | NCBI36 |
NG_008358.1:g.9132_9133insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.*57_*58insA | ENSP00000372295.1:n.*57_*58insA | |
ENST00000382848.5:c.*57_*58insA MANE Select | ENSP00000372299.4:n.*57_*58insA | |
ENST00000382844.1:c.*57_*58insA | ENSP00000372295.1:n.*57_*58insA | |
ENST00000382848.4:c.*57_*58insA | ENSP00000372299.4:n.*57_*58insA | |
NM_004004.5:c.*57_*58insA | NP_003995.2:n.*57_*58insA | |
XM_011535049.1:c.*57_*58insA | XP_011533351.1:n.*57_*58insA | |
XM_011535049.2:c.*57_*58insA | XP_011533351.1:n.*57_*58insA | |
NM_004004.6:c.*57_*58insA MANE Select | NP_003995.2:n.*57_*58insA |