HGVS | Genome Assembly |
---|---|
NC_000017.11:g.30216253_30216289del , CM000679.2:g.30216253_30216289del | GRCh38 |
NC_000017.10:g.28543271_28543307del , CM000679.1:g.28543271_28543307del | GRCh37 |
NC_000017.9:g.25567397_25567433del | NCBI36 |
NG_011747.2:g.24650_24686del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650711.1:c.838-71_838-35del MANE Select | ENSP00000498537.1:n.838-71_838-35del | |
ENST00000261707.7:c.838-71_838-35del | ENSP00000261707.3:n.838-71_838-35del | |
ENST00000394821.2:c.838-71_838-35del | ENSP00000378298.2:n.838-71_838-35del | |
ENST00000401766.6:c.838-71_838-35del | ENSP00000385822.2:n.838-71_838-35del | |
NM_001045.5:c.838-71_838-35del | NP_001036.1:n.838-71_838-35del | |
NM_001045.6:c.838-71_838-35del MANE Select | NP_001036.1:n.838-71_838-35del |