HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18400193_18400194delinsT , CM000670.2:g.18400193_18400194delinsT | GRCh38 |
NC_000008.10:g.18257703_18257704delinsT , CM000670.1:g.18257703_18257704delinsT | GRCh37 |
NC_000008.9:g.18301983_18301984delinsT | NCBI36 |
NG_012246.1:g.13949_13950delinsT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000286479.4:c.190_191delinsT MANE Select | ENSP00000286479.3:p.Arg64TrpfsTer16 | |
ENST00000286479.3:c.190_191delinsT | ENSP00000286479.3:p.Arg64TrpfsTer16 | |
ENST00000520116.1:c.-57-144_-57-143delinsT | ENSP00000428416.1:n.-57-144_-57-143delinsT | |
NM_000015.2:c.190_191delinsT | NP_000006.2:p.Arg64TrpfsTer16 | |
XM_011544358.1:c.190_191delinsT | XP_011542660.1:p.Arg64TrpfsTer16 | |
XM_017012938.1:c.190_191delinsT | XP_016868427.1:p.Arg64TrpfsTer16 | |
NM_000015.3:c.190_191delinsT MANE Select | NP_000006.2:p.Arg64TrpfsTer16 |