HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7454394_7454395delinsCA , CM000679.2:g.7454394_7454395delinsCA | GRCh38 |
NC_000017.10:g.7357713_7357714delinsCA , CM000679.1:g.7357713_7357714delinsCA | GRCh37 |
NC_000017.9:g.7298437_7298438delinsCA | NCBI36 |
NG_008026.1:g.14308_14309delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000306071.7:c.918_919delinsCA MANE Select | ENSP00000304290.2:p.Pro306= | |
ENST00000306071.6:c.918_919delinsCA | ENSP00000304290.2:p.Pro306= | |
ENST00000536404.6:c.702_703delinsCA | ENSP00000439209.2:p.Pro234= | |
ENST00000570557.5:c.581_582delinsCA | ||
ENST00000573209.1:n.1862_1863delinsCA | ||
ENST00000576360.1:c.605-50_605-49delinsCA | ENSP00000459092.1:n.605-50_605-49delinsCA | |
NM_000747.2:c.918_919delinsCA | NP_000738.2:p.Pro306= | |
NM_000747.3:c.918_919delinsCA MANE Select | NP_000738.2:p.Pro306= |