HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47286308_47286312delinsGCTAA , CM000679.2:g.47286308_47286312delinsGCTAA | GRCh38 |
NC_000017.10:g.45363674_45363678delinsGCTAA , CM000679.1:g.45363674_45363678delinsGCTAA | GRCh37 |
NC_000017.9:g.42718673_42718677delinsGCTAA | NCBI36 |
NG_008332.2:g.37467_37471delinsGCTAA , LRG_481:g.37467_37471delinsGCTAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696963.1:c.663_667delinsGCTAA | ENSP00000513002.1:p.Thr221= | |
ENST00000559488.7:c.663_667delinsGCTAA MANE Select | ENSP00000452786.2:p.Thr221= | |
ENST00000559488.5:c.663_667delinsGCTAA | ENSP00000452786.1:p.Thr221= | |
ENST00000560629.1:c.628_632delinsGCTAA | ||
ENST00000571680.1:c.663_667delinsGCTAA | ENSP00000461626.1:p.Thr221= | |
NM_000212.2:c.663_667delinsGCTAA , LRG_481t1:c.663_667delinsGCTAA | NP_000203.2:p.Thr221= | |
NM_000212.3:c.663_667delinsGCTAA MANE Select | NP_000203.2:p.Thr221= |