HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269109del , CM000668.2:g.31269109del | GRCh38 |
NC_000006.11:g.31236886del , CM000668.1:g.31236886del | GRCh37 |
NC_000006.10:g.31344865del | NCBI36 |
NG_029422.2:g.8023del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.*60del MANE Select | ENSP00000365402.5:n.*60del | |
ENST00000376228.9:c.*60del | ENSP00000365402.5:n.*60del | |
ENST00000376237.8:c.*748del | ENSP00000365412.4:n.*748del | |
ENST00000383329.7:c.*60del | ENSP00000372819.3:n.*60del | |
ENST00000466892.5:n.394del | ||
ENST00000470363.5:n.919del | ||
ENST00000487245.5:n.1520del | ||
NM_002117.5:c.*60del | NP_002108.4:n.*60del | |
NM_002117.6:c.*60del MANE Select | NP_002108.4:n.*60del |