HGVS | Genome Assembly |
---|---|
NC_000009.12:g.137199337del , CM000671.2:g.137199337del | GRCh38 |
NC_000009.11:g.140093789del , CM000671.1:g.140093789del | GRCh37 |
NC_000009.10:g.139213610del | NCBI36 |
NG_027801.1:g.6375del | |
NG_027801.2:g.9857del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409012.6:c.1375del MANE Select | ENSP00000387100.4:p.Asp459MetfsTer3 | |
ENST00000333046.8:c.769del | ENSP00000327617.4:p.Asp257MetfsTer3 | |
ENST00000409012.4:c.1375del | ENSP00000387100.4:p.Asp459MetfsTer3 | |
ENST00000541945.1:n.90+4767del | ||
NM_001128228.2:c.1375del | NP_001121700.2:p.Asp459MetfsTer3 | |
NM_001128228.3:c.1375del MANE Select | NP_001121700.2:p.Asp459MetfsTer3 |