HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31271254del , CM000668.2:g.31271254del | GRCh38 |
NC_000006.11:g.31239031del , CM000668.1:g.31239031del | GRCh37 |
NC_000006.10:g.31347010del | NCBI36 |
NG_029422.2:g.5879del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.439del MANE Select | ENSP00000365402.5:p.Tyr147ThrfsTer4 | |
ENST00000376228.9:c.439del | ENSP00000365402.5:p.Tyr147ThrfsTer4 | |
ENST00000376237.8:c.*26del | ENSP00000365412.4:n.*26del | |
ENST00000383329.7:c.439del | ENSP00000372819.3:p.Tyr147ThrfsTer4 | |
ENST00000415537.1:c.437del | ||
ENST00000484378.1:n.708del | ||
ENST00000487245.5:n.798del | ||
ENST00000495835.1:n.628del | ||
NM_002117.5:c.439del | NP_002108.4:p.Tyr147ThrfsTer4 | |
NM_002117.6:c.439del MANE Select | NP_002108.4:p.Tyr147ThrfsTer4 |