HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734371_4734410dup , CM000679.2:g.4734371_4734410dup | GRCh38 |
NC_000017.10:g.4637666_4637705dup , CM000679.1:g.4637666_4637705dup | GRCh37 |
NC_000017.9:g.4584415_4584454dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*93_*132dup MANE Select | ENSP00000293778.7:n.*93_*132dup | |
ENST00000574412.6:c.*196_*235dup | ENSP00000459592.2:n.*196_*235dup | |
ENST00000293778.10:c.*93_*132dup | ENSP00000293778.6:n.*93_*132dup | |
ENST00000574412.5:c.*196_*235dup | ENSP00000459592.1:n.*196_*235dup | |
ENST00000576153.5:n.649_688dup | ||
NM_022059.3:c.*93_*132dup | NP_071342.2:n.*93_*132dup | |
NM_022059.4:c.*93_*132dup | NP_071342.2:n.*93_*132dup | |
NM_001386809.1:c.*93_*132dup MANE Select | NP_001373738.1:n.*93_*132dup |