HGVS | Genome Assembly |
---|---|
NC_000023.11:g.21845318_21845335del , CM000685.2:g.21845318_21845335del | GRCh38 |
NC_000023.10:g.21863436_21863453del , CM000685.1:g.21863436_21863453del | GRCh37 |
NC_000023.9:g.21773357_21773374del | NCBI36 |
NG_012797.1:g.10781_10798del | |
NG_012797.2:g.10781_10798del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379484.10:c.372_389del MANE Select | ENSP00000368798.5:p.Ser125_Ser130del | |
ENST00000365779.2:c.372_389del | ENSP00000368796.1:p.Ser125_Ser130del | |
ENST00000379484.9:c.372_389del | ENSP00000368798.5:p.Ser125_Ser130del | |
ENST00000465888.1:n.471_488del | ||
NM_015884.3:c.372_389del | NP_056968.1:p.Ser125_Ser130del | |
NM_015884.4:c.372_389del MANE Select | NP_056968.1:p.Ser125_Ser130del |