HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625363_22625376del , CM000673.2:g.22625363_22625376del | GRCh38 |
NC_000011.9:g.22646909_22646922del , CM000673.1:g.22646909_22646922del | GRCh37 |
NC_000011.8:g.22603485_22603498del | NCBI36 |
NG_007425.1:g.5469_5482del , LRG_527:g.5469_5482del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.438_451del MANE Select | ENSP00000330875.3:p.Arg147Ter | |
ENST00000327470.4:c.438_451del | ENSP00000330875.3:p.Arg147Ter | |
NM_022725.3:c.438_451del , LRG_527t1:c.438_451del | NP_073562.1:p.Arg147Ter | |
NM_022725.4:c.438_451del MANE Select | NP_073562.1:p.Arg147Ter |