HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31271222del , CM000668.2:g.31271222del | GRCh38 |
NC_000006.11:g.31238999del , CM000668.1:g.31238999del | GRCh37 |
NC_000006.10:g.31346978del | NCBI36 |
NG_029422.2:g.5911del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.471del MANE Select | ENSP00000365402.5:p.Trp157Ter | |
ENST00000376228.9:c.471del | ENSP00000365402.5:p.Trp157Ter | |
ENST00000376237.8:c.*58del | ENSP00000365412.4:n.*58del | |
ENST00000383329.7:c.471del | ENSP00000372819.3:p.Trp157Ter | |
ENST00000415537.1:c.469del | ||
ENST00000484378.1:n.740del | ||
ENST00000487245.5:n.830del | ||
ENST00000495835.1:n.660del | ||
NM_002117.5:c.471del | NP_002108.4:p.Trp157Ter | |
NM_002117.6:c.471del MANE Select | NP_002108.4:p.Trp157Ter |