HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18787508_18787513del , CM000681.2:g.18787508_18787513del | GRCh38 |
NC_000019.9:g.18898317_18898322del , CM000681.1:g.18898317_18898322del | GRCh37 |
NC_000019.8:g.18759317_18759322del | NCBI36 |
NG_007070.1:g.8797_8802del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.1117_1122del MANE Select | ENSP00000222271.2:p.Asp373_Asp374del | |
ENST00000222271.6:c.1117_1122del | ENSP00000222271.2:p.Asp373_Asp374del | |
ENST00000425807.1:c.958_963del | ENSP00000403792.1:p.Asp320_Asp321del | |
ENST00000542601.6:c.1018_1023del | ENSP00000439156.2:p.Asp340_Asp341del | |
NM_000095.2:c.1117_1122del | NP_000086.2:p.Asp373_Asp374del | |
NM_000095.3:c.1117_1122del MANE Select | NP_000086.2:p.Asp373_Asp374del |