HGVS | Genome Assembly |
---|---|
NC_000017.11:g.30221468_30221505del , CM000679.2:g.30221468_30221505del | GRCh38 |
NC_000017.10:g.28548486_28548523del , CM000679.1:g.28548486_28548523del | GRCh37 |
NC_000017.9:g.25572612_25572649del | NCBI36 |
NG_011747.2:g.19433_19470del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650711.1:c.343+112_343+149del MANE Select | ENSP00000498537.1:n.343+112_343+149del | |
ENST00000261707.7:c.343+112_343+149del | ENSP00000261707.3:n.343+112_343+149del | |
ENST00000394821.2:c.343+112_343+149del | ENSP00000378298.2:n.343+112_343+149del | |
ENST00000401766.6:c.343+112_343+149del | ENSP00000385822.2:n.343+112_343+149del | |
NM_001045.5:c.343+112_343+149del | NP_001036.1:n.343+112_343+149del | |
NM_001045.6:c.343+112_343+149del MANE Select | NP_001036.1:n.343+112_343+149del |