HGVS | Genome Assembly |
---|---|
NC_000023.11:g.21845348_21845353del , CM000685.2:g.21845348_21845353del | GRCh38 |
NC_000023.10:g.21863466_21863471del , CM000685.1:g.21863466_21863471del | GRCh37 |
NC_000023.9:g.21773387_21773392del | NCBI36 |
NG_012797.1:g.10811_10816del | |
NG_012797.2:g.10811_10816del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379484.10:c.402_407del MANE Select | ENSP00000368798.5:p.Ser135_Ser136del | |
ENST00000365779.2:c.402_407del | ENSP00000368796.1:p.Ser135_Ser136del | |
ENST00000379484.9:c.402_407del | ENSP00000368798.5:p.Ser135_Ser136del | |
ENST00000465888.1:n.501_506del | ||
NM_015884.3:c.402_407del | NP_056968.1:p.Ser135_Ser136del | |
NM_015884.4:c.402_407del MANE Select | NP_056968.1:p.Ser135_Ser136del |