HGVS | Genome Assembly |
---|---|
NC_000023.11:g.21845312_21845329del , CM000685.2:g.21845312_21845329del | GRCh38 |
NC_000023.10:g.21863430_21863447del , CM000685.1:g.21863430_21863447del | GRCh37 |
NC_000023.9:g.21773351_21773368del | NCBI36 |
NG_012797.1:g.10775_10792del | |
NG_012797.2:g.10775_10792del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000379484.10:c.366_383del MANE Select | ENSP00000368798.5:p.Ser123_Ser128del | |
ENST00000365779.2:c.366_383del | ENSP00000368796.1:p.Ser123_Ser128del | |
ENST00000379484.9:c.366_383del | ENSP00000368798.5:p.Ser123_Ser128del | |
ENST00000465888.1:n.465_482del | ||
NM_015884.3:c.366_383del | NP_056968.1:p.Ser123_Ser128del | |
NM_015884.4:c.366_383del MANE Select | NP_056968.1:p.Ser123_Ser128del |