HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104057065_104057066insA , CM000672.2:g.104057065_104057066insA | GRCh38 |
NC_000010.10:g.105816823_105816824insA , CM000672.1:g.105816823_105816824insA | GRCh37 |
NC_000010.9:g.105806813_105806814insA | NCBI36 |
NG_007069.1:g.33815_33816insT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369733.8:c.1374_1375insT | ENSP00000358748.3:p.Gly459TrpfsTer? | |
ENST00000648076.2:c.1374_1375insT MANE Select | ENSP00000497653.1:p.Gly459TrpfsTer? | |
ENST00000650263.1:c.1326_1327insT | ENSP00000497850.1:p.Gly443TrpfsTer? | |
ENST00000353479.9:c.1374_1375insT | ENSP00000340937.5:p.Gly459TrpfsTer? | |
ENST00000369733.7:c.1374_1375insT | ENSP00000358748.3:p.Gly459TrpfsTer? | |
NM_000494.3:c.1374_1375insT | NP_000485.3:p.Gly459TrpfsTer? | |
NM_000494.4:c.1374_1375insT MANE Select | NP_000485.3:p.Gly459TrpfsTer? |