HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31268822dup , CM000668.2:g.31268822dup | GRCh38 |
NC_000006.11:g.31236599dup , CM000668.1:g.31236599dup | GRCh37 |
NC_000006.10:g.31344578dup | NCBI36 |
NG_029422.2:g.8310dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.*347dup MANE Select | ENSP00000365402.5:n.*347dup | |
ENST00000376228.9:c.*347dup | ENSP00000365402.5:n.*347dup | |
ENST00000376237.8:c.*1035dup | ENSP00000365412.4:n.*1035dup | |
ENST00000383329.7:c.*347dup | ENSP00000372819.3:n.*347dup | |
ENST00000466892.5:n.681dup | ||
ENST00000470363.5:n.1206dup | ||
ENST00000487245.5:n.1807dup | ||
NM_002117.5:c.*347dup | NP_002108.4:n.*347dup | |
NM_002117.6:c.*347dup MANE Select | NP_002108.4:n.*347dup |