HGVS | Genome Assembly |
---|---|
NC_000017.11:g.82727631_82727641del , CM000679.2:g.82727631_82727641del | GRCh38 |
NC_000017.10:g.80685507_80685517del , CM000679.1:g.80685507_80685517del | GRCh37 |
NC_000017.9:g.78278796_78278806del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000269373.11:c.*460_*470del MANE Select | ENSP00000269373.6:n.*460_*470del | |
ENST00000269373.10:c.*460_*470del | ENSP00000269373.6:n.*460_*470del | |
ENST00000571594.1:c.53+464_53+474del | ENSP00000459751.1:n.53+464_53+474del | |
NM_024619.3:c.*460_*470del | NP_078895.2:n.*460_*470del | |
NR_046408.1:n.1568_1578del | ||
XM_024450948.1:c.*460_*470del | XP_024306716.1:n.*460_*470del | |
NM_024619.4:c.*460_*470del MANE Select | NP_078895.2:n.*460_*470del | |
NR_046408.2:n.1568_1578del |