HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148994652_148994655delinsTTGG , CM000667.2:g.148994652_148994655delinsTTGG | GRCh38 |
NC_000005.9:g.148374215_148374218delinsTTGG , CM000667.1:g.148374215_148374218delinsTTGG | GRCh37 |
NC_000005.8:g.148354408_148354411delinsTTGG | NCBI36 |
NG_007947.2:g.73520_73523delinsCCAA , LRG_269:g.73520_73523delinsCCAA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000515425.6:c.*10056_*10059delinsCCAA MANE Select | ENSP00000423660.1:n.*10056_*10059delinsCCAA | |
ENST00000504690.5:c.*12+9071_*12+9074delinsCCAA | ENSP00000425627.1:n.*12+9071_*12+9074delinsCCAA | |
ENST00000510350.1:n.231+12226_231+12229delinsCCAA | ||
NM_024577.3:c.*10056_*10059delinsCCAA , LRG_269t1:c.*10056_*10059delinsCCAA | NP_078853.2:n.*10056_*10059delinsCCAA | |
NM_024577.4:c.*10056_*10059delinsCCAA MANE Select | NP_078853.2:n.*10056_*10059delinsCCAA |