HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55039621_55039632del , CM000663.2:g.55039621_55039632del | GRCh38 |
NC_000001.10:g.55505294_55505305del , CM000663.1:g.55505294_55505305del | GRCh37 |
NC_000001.9:g.55277882_55277893del | NCBI36 |
NG_009061.1:g.5075_5086del , LRG_275:g.5075_5086del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673913.2:c.-217_-206del | ENSP00000501161.2:n.-217_-206del | |
ENST00000710286.1:c.141_152del | ENSP00000518176.1:p.Ser47_Val50del | |
ENST00000673726.1:c.-217_-206del | ENSP00000501004.1:n.-217_-206del | |
ENST00000302118.5:c.-217_-206del MANE Select | ENSP00000303208.5:n.-217_-206del | |
NM_174936.3:c.-217_-206del , LRG_275t1:c.-217_-206del | NP_777596.2:n.-217_-206del | |
NM_174936.4:c.-217_-206del MANE Select | NP_777596.2:n.-217_-206del |