HGVS | Genome Assembly |
---|---|
NC_000012.12:g.20368724_20368728delinsGAGAA , CM000674.2:g.20368724_20368728delinsGAGAA | GRCh38 |
NC_000012.11:g.20521658_20521662delinsGAGAA , CM000674.1:g.20521658_20521662delinsGAGAA | GRCh37 |
NC_000012.10:g.20412925_20412929delinsGAGAA | NCBI36 |
NG_030033.1:g.4480_4484delinsGAGAA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000359062.4:c.-561_-557delinsGAGAA MANE Select | ENSP00000351957.3:n.-561_-557delinsGAGAA | |
XM_006719086.2:c.-561_-557delinsGAGAA | XP_006719149.2:n.-561_-557delinsGAGAA | |
NM_000921.5:c.-561_-557delinsGAGAA MANE Select | NP_000912.3:n.-561_-557delinsGAGAA | |
NM_001378407.1:c.-561_-557delinsGAGAA | NP_001365336.1:n.-561_-557delinsGAGAA | |
NM_001378408.1:c.-1589_-1585delinsGAGAA | NP_001365337.1:n.-1589_-1585delinsGAGAA |