HGVS | Genome Assembly |
---|---|
NC_000011.10:g.6319436_6319457del , CM000673.2:g.6319436_6319457del | GRCh38 |
NC_000011.9:g.6340666_6340687del , CM000673.1:g.6340666_6340687del | GRCh37 |
NC_000011.8:g.6297242_6297263del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303927.4:c.495_516del MANE Select | ENSP00000307292.3:p.Ser166ProfsTer? | |
ENST00000303927.3:c.495_516del | ENSP00000307292.3:p.Ser166ProfsTer? | |
ENST00000524852.1:n.281_302del | ||
ENST00000530979.1:c.591_612del | ENSP00000432047.1:p.Ser198ProfsTer? | |
ENST00000532354.1:n.517_538del | ||
NM_145040.2:c.495_516del | NP_659477.2:p.Ser166ProfsTer? | |
XR_930997.1:n.720+1216_720+1237del | ||
XR_001748106.1:n.47_68del | ||
XR_242848.4:n.296_317del | ||
NM_145040.3:c.495_516del MANE Select | NP_659477.2:p.Ser166ProfsTer? |