HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229432455_229432458del , CM000663.2:g.229432455_229432458del | GRCh38 |
NC_000001.10:g.229568202_229568205del , CM000663.1:g.229568202_229568205del | GRCh37 |
NC_000001.9:g.227634825_227634828del | NCBI36 |
NG_006672.1:g.6644_6647del , LRG_429:g.6644_6647del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366683.4:c.455-22_455-19del | ENSP00000355644.4:n.455-22_455-19del | |
ENST00000684723.1:c.320-22_320-19del | ENSP00000508084.1:n.320-22_320-19del | |
ENST00000366683.3:c.455-22_455-19del | ENSP00000355644.3:n.455-22_455-19del | |
ENST00000366684.7:c.455-22_455-19del MANE Select | ENSP00000355645.3:n.455-22_455-19del | |
NM_001100.3:c.455-22_455-19del , LRG_429t1:c.455-22_455-19del | NP_001091.1:n.455-22_455-19del | |
NM_001100.4:c.455-22_455-19del MANE Select | NP_001091.1:n.455-22_455-19del |