HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98364015_98364018delinsATTC , CM000669.2:g.98364015_98364018delinsATTC | GRCh38 |
NC_000007.13:g.97993327_97993330delinsATTC , CM000669.1:g.97993327_97993330delinsATTC | GRCh37 |
NC_000007.12:g.97831263_97831266delinsATTC | NCBI36 |
NG_013090.1:g.42098_42101delinsGAAT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000005260.9:c.52-1586_52-1583delinsGAAT MANE Select | ENSP00000005260.8:n.52-1586_52-1583delinsGAAT | |
ENST00000005260.8:c.52-1586_52-1583delinsGAAT | ENSP00000005260.8:n.52-1586_52-1583delinsGAAT | |
ENST00000462558.5:n.268-1586_268-1583delinsGAAT | ||
ENST00000479789.1:n.358-1586_358-1583delinsGAAT | ||
NM_018842.4:c.52-1586_52-1583delinsGAAT | NP_061330.2:n.52-1586_52-1583delinsGAAT | |
NM_018842.5:c.52-1586_52-1583delinsGAAT MANE Select | NP_061330.2:n.52-1586_52-1583delinsGAAT |