HGVS | Genome Assembly |
---|---|
NC_000010.11:g.30313871del , CM000672.2:g.30313871del | GRCh38 |
NC_000010.10:g.30602800del , CM000672.1:g.30602800del | GRCh37 |
NC_000010.9:g.30642806del | NCBI36 |
NG_028096.1:g.40472del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263063.9:c.1491del MANE Select | ENSP00000263063.3:p.Lys497AsnfsTer3 | |
ENST00000263063.8:c.1491del | ENSP00000263063.3:p.Lys497AsnfsTer3 | |
ENST00000488290.5:n.3246del | ||
NM_018109.3:c.1491del | NP_060579.3:p.Lys497AsnfsTer3 | |
NM_018109.4:c.1491del MANE Select | NP_060579.3:p.Lys497AsnfsTer3 |