HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625417_22625454del , CM000673.2:g.22625417_22625454del | GRCh38 |
NC_000011.9:g.22646963_22647000del , CM000673.1:g.22646963_22647000del | GRCh37 |
NC_000011.8:g.22603539_22603576del | NCBI36 |
NG_007425.1:g.5389_5426del , LRG_527:g.5389_5426del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.358_395del MANE Select | ENSP00000330875.3:p.Gly120ProfsTer20 | |
ENST00000327470.4:c.358_395del | ENSP00000330875.3:p.Gly120ProfsTer20 | |
NM_022725.3:c.358_395del , LRG_527t1:c.358_395del | NP_073562.1:p.Gly120ProfsTer20 | |
NM_022725.4:c.358_395del MANE Select | NP_073562.1:p.Gly120ProfsTer20 |