HGVS | Genome Assembly |
---|---|
NC_000017.11:g.44372311del , CM000679.2:g.44372311del | GRCh38 |
NC_000017.10:g.42449679del , CM000679.1:g.42449679del | GRCh37 |
NC_000017.9:g.39805205del | NCBI36 |
NG_008331.1:g.22198del , LRG_479:g.22198del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262407.6:c.*56del MANE Select | ENSP00000262407.5:n.*56del | |
ENST00000648408.1:c.2490del | ||
ENST00000262407.5:c.*56del | ENSP00000262407.5:n.*56del | |
ENST00000587295.5:c.369del | ||
ENST00000588098.1:c.153del | ||
NM_000419.3:c.*56del , LRG_479t1:c.*56del | NP_000410.2:n.*56del | |
XM_011524749.1:c.*56del | XP_011523051.1:n.*56del | |
XM_011524750.1:c.*56del | XP_011523052.1:n.*56del | |
NM_000419.4:c.*56del | NP_000410.2:n.*56del | |
NM_000419.5:c.*56del MANE Select | NP_000410.2:n.*56del |