HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47284647_47284648delinsCA , CM000679.2:g.47284647_47284648delinsCA | GRCh38 |
NC_000017.10:g.45362013_45362014delinsCA , CM000679.1:g.45362013_45362014delinsCA | GRCh37 |
NC_000017.9:g.42717012_42717013delinsCA | NCBI36 |
NG_008332.2:g.35806_35807delinsCA , LRG_481:g.35806_35807delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696963.1:c.566_567delinsCA | ENSP00000513002.1:p.Pro189= | |
ENST00000559488.7:c.566_567delinsCA MANE Select | ENSP00000452786.2:p.Pro189= | |
ENST00000559488.5:c.566_567delinsCA | ENSP00000452786.1:p.Pro189= | |
ENST00000560629.1:c.531_532delinsCA | ||
ENST00000571680.1:c.566_567delinsCA | ENSP00000461626.1:p.Pro189= | |
NM_000212.2:c.566_567delinsCA , LRG_481t1:c.566_567delinsCA | NP_000203.2:p.Pro189= | |
NM_000212.3:c.566_567delinsCA MANE Select | NP_000203.2:p.Pro189= |