HGVS | Genome Assembly |
---|---|
NC_000016.10:g.173069del , CM000678.2:g.173069del | GRCh38 |
NC_000016.9:g.223068del , CM000678.1:g.223068del | GRCh37 |
NC_000016.8:g.163068del | NCBI36 |
NG_000006.1:g.33932del | |
NG_059186.1:g.1419del | |
NG_059271.1:g.5223del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251595.11:c.96-56del MANE Select | ENSP00000251595.6:n.96-56del | |
ENST00000251595.10:c.96-56del | ENSP00000251595.6:n.96-56del | |
ENST00000397806.1:c.-1-56del | ENSP00000380908.1:n.-1-56del | |
ENST00000482565.1:n.176del | ||
ENST00000484216.1:n.65-56del | ||
NM_000517.4:c.96-56del | NP_000508.1:n.96-56del | |
NM_000517.6:c.96-56del MANE Select | NP_000508.1:n.96-56del |