HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225647_3225649del , CM000668.2:g.3225647_3225649del | GRCh38 |
NC_000006.11:g.3225881_3225883del , CM000668.1:g.3225881_3225883del | GRCh37 |
NC_000006.10:g.3170880_3170882del | NCBI36 |
NG_016715.1:g.7086_7088del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.440_442del MANE Select | ENSP00000259818.6:p.Met147_Gly148delinsSer | |
ENST00000680070.1:n.1370_1372del | ||
ENST00000681707.1:n.1267_1269del | ||
ENST00000681757.1:n.745_747del | ||
ENST00000259818.7:c.440_442del | ENSP00000259818.6:p.Met147_Gly148delinsSer | |
ENST00000473006.1:n.557_559del | ||
NM_178012.4:c.440_442del | NP_821080.1:p.Met147_Gly148delinsSer | |
XM_011514571.1:c.224_226del | XP_011512873.1:p.Met75_Gly76delinsSer | |
NM_178012.5:c.440_442del MANE Select | NP_821080.1:p.Met147_Gly148delinsSer |