HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225631_3225633del , CM000668.2:g.3225631_3225633del | GRCh38 |
NC_000006.11:g.3225865_3225867del , CM000668.1:g.3225865_3225867del | GRCh37 |
NC_000006.10:g.3170864_3170866del | NCBI36 |
NG_016715.1:g.7104_7106del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.458_460del MANE Select | ENSP00000259818.6:p.Ser153del | |
ENST00000680070.1:n.1388_1390del | ||
ENST00000681707.1:n.1285_1287del | ||
ENST00000681757.1:n.763_765del | ||
ENST00000259818.7:c.458_460del | ENSP00000259818.6:p.Ser153del | |
ENST00000473006.1:n.575_577del | ||
NM_178012.4:c.458_460del | NP_821080.1:p.Ser153del | |
XM_011514571.1:c.242_244del | XP_011512873.1:p.Ser81del | |
NM_178012.5:c.458_460del MANE Select | NP_821080.1:p.Ser153del |