HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734107_4734108insCTG , CM000679.2:g.4734107_4734108insCTG | GRCh38 |
NC_000017.10:g.4637402_4637403insCTG , CM000679.1:g.4637402_4637403insCTG | GRCh37 |
NC_000017.9:g.4584151_4584152insCTG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*396_*397insAGC MANE Select | ENSP00000293778.7:n.*396_*397insAGC | |
ENST00000293778.10:c.*396_*397insAGC | ENSP00000293778.6:n.*396_*397insAGC | |
ENST00000576153.5:n.952_953insAGC | ||
NM_022059.3:c.*396_*397insAGC | NP_071342.2:n.*396_*397insAGC | |
NM_022059.4:c.*396_*397insAGC | NP_071342.2:n.*396_*397insAGC | |
NM_001386809.1:c.*396_*397insAGC MANE Select | NP_001373738.1:n.*396_*397insAGC |