HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98363990_98363991delinsTG , CM000669.2:g.98363990_98363991delinsTG | GRCh38 |
NC_000007.13:g.97993302_97993303delinsTG , CM000669.1:g.97993302_97993303delinsTG | GRCh37 |
NC_000007.12:g.97831238_97831239delinsTG | NCBI36 |
NG_013090.1:g.42125_42126delinsCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000005260.9:c.52-1559_52-1558delinsCA MANE Select | ENSP00000005260.8:n.52-1559_52-1558delinsCA | |
ENST00000005260.8:c.52-1559_52-1558delinsCA | ENSP00000005260.8:n.52-1559_52-1558delinsCA | |
ENST00000462558.5:n.268-1559_268-1558delinsCA | ||
ENST00000479789.1:n.358-1559_358-1558delinsCA | ||
NM_018842.4:c.52-1559_52-1558delinsCA | NP_061330.2:n.52-1559_52-1558delinsCA | |
NM_018842.5:c.52-1559_52-1558delinsCA MANE Select | NP_061330.2:n.52-1559_52-1558delinsCA |