HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31271357del , CM000668.2:g.31271357del | GRCh38 |
NC_000006.11:g.31239134del , CM000668.1:g.31239134del | GRCh37 |
NC_000006.10:g.31347113del | NCBI36 |
NG_029422.2:g.5775del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.344-9del MANE Select | ENSP00000365402.5:n.344-9del | |
ENST00000376228.9:c.344-9del | ENSP00000365402.5:n.344-9del | |
ENST00000376237.8:c.344-26del | ENSP00000365412.4:n.344-26del | |
ENST00000383329.7:c.344-9del | ENSP00000372819.3:n.344-9del | |
ENST00000415537.1:c.342-9del | ||
ENST00000484378.1:n.604del | ||
ENST00000487245.5:n.694del | ||
ENST00000495835.1:n.533-9del | ||
NM_002117.5:c.344-9del | NP_002108.4:n.344-9del | |
NM_002117.6:c.344-9del MANE Select | NP_002108.4:n.344-9del |