HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734255_4734258delinsGTTA , CM000679.2:g.4734255_4734258delinsGTTA | GRCh38 |
NC_000017.10:g.4637550_4637553delinsGTTA , CM000679.1:g.4637550_4637553delinsGTTA | GRCh37 |
NC_000017.9:g.4584299_4584302delinsGTTA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*245_*248delinsTAAC MANE Select | ENSP00000293778.7:n.*245_*248delinsTAAC | |
ENST00000293778.10:c.*245_*248delinsTAAC | ENSP00000293778.6:n.*245_*248delinsTAAC | |
ENST00000576153.5:n.801_804delinsTAAC | ||
NM_022059.3:c.*245_*248delinsTAAC | NP_071342.2:n.*245_*248delinsTAAC | |
NM_022059.4:c.*245_*248delinsTAAC | NP_071342.2:n.*245_*248delinsTAAC | |
NM_001386809.1:c.*245_*248delinsTAAC MANE Select | NP_001373738.1:n.*245_*248delinsTAAC |