HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19957479_19957481delinsTAA , CM000670.2:g.19957479_19957481delinsTAA | GRCh38 |
NC_000008.10:g.19814990_19814992delinsTAA , CM000670.1:g.19814990_19814992delinsTAA | GRCh37 |
NC_000008.9:g.19859270_19859272delinsTAA | NCBI36 |
NG_008855.1:g.23409_23411delinsTAA | |
NG_008855.2:g.60763_60765delinsTAA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.1018+1396_1018+1398delinsTAA MANE Select | ENSP00000497642.1:n.1018+1396_1018+1398de... | |
ENST00000650478.1:c.79+1396_79+1398delinsTAA | ENSP00000497560.1:n.79+1396_79+1398delins... | |
ENST00000311322.8:c.1018+1396_1018+1398delinsTAA | ENSP00000309757.6:n.1018+1396_1018+1398de... | |
NM_000237.2:c.1018+1396_1018+1398delinsTAA | NP_000228.1:n.1018+1396_1018+1398delinsTA... | |
NM_000237.3:c.1018+1396_1018+1398delinsTAA MANE Select | NP_000228.1:n.1018+1396_1018+1398delinsTA... |