HGVS | Genome Assembly |
---|---|
NC_000023.11:g.74421760_74421771del , CM000685.2:g.74421760_74421771del | GRCh38 |
NC_000023.10:g.73641595_73641606del , CM000685.1:g.73641595_73641606del | GRCh37 |
NC_000023.9:g.73558320_73558331del | NCBI36 |
NG_011641.1:g.5511_5522del | |
NG_011641.2:g.5511_5522del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000587091.6:c.123_134del MANE Select | ENSP00000465734.1:p.Glu42_Pro45del | |
ENST00000587091.5:c.123_134del | ENSP00000465734.1:p.Glu42_Pro45del | |
NM_006517.4:c.123_134del | NP_006508.2:p.Glu42_Pro45del | |
XM_005262294.1:c.123_134del | XP_005262351.1:p.Glu42_Pro45del | |
XM_011531015.1:c.123_134del | XP_011529317.1:p.Glu42_Pro45del | |
NM_006517.5:c.123_134del MANE Select | NP_006508.2:p.Glu42_Pro45del |