HGVS | Genome Assembly |
---|---|
NC_000012.12:g.20368732_20368734delinsAAG , CM000674.2:g.20368732_20368734delinsAAG | GRCh38 |
NC_000012.11:g.20521666_20521668delinsAAG , CM000674.1:g.20521666_20521668delinsAAG | GRCh37 |
NC_000012.10:g.20412933_20412935delinsAAG | NCBI36 |
NG_030033.1:g.4488_4490delinsAAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000359062.4:c.-553_-551delinsAAG MANE Select | ENSP00000351957.3:n.-553_-551delinsAAG | |
XM_006719086.2:c.-553_-551delinsAAG | XP_006719149.2:n.-553_-551delinsAAG | |
NM_000921.5:c.-553_-551delinsAAG MANE Select | NP_000912.3:n.-553_-551delinsAAG | |
NM_001378407.1:c.-553_-551delinsAAG | NP_001365336.1:n.-553_-551delinsAAG | |
NM_001378408.1:c.-1581_-1579delinsAAG | NP_001365337.1:n.-1581_-1579delinsAAG |