HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734099_4734100insAGC , CM000679.2:g.4734099_4734100insAGC | GRCh38 |
NC_000017.10:g.4637394_4637395insAGC , CM000679.1:g.4637394_4637395insAGC | GRCh37 |
NC_000017.9:g.4584143_4584144insAGC | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*404_*405insCTG MANE Select | ENSP00000293778.7:n.*404_*405insCTG | |
ENST00000293778.10:c.*404_*405insCTG | ENSP00000293778.6:n.*404_*405insCTG | |
ENST00000576153.5:n.960_961insCTG | ||
NM_022059.3:c.*404_*405insCTG | NP_071342.2:n.*404_*405insCTG | |
NM_022059.4:c.*404_*405insCTG | NP_071342.2:n.*404_*405insCTG | |
NM_001386809.1:c.*404_*405insCTG MANE Select | NP_001373738.1:n.*404_*405insCTG |