HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160881828_160881829insGTG , CM000663.2:g.160881828_160881829insGTG | GRCh38 |
NC_000001.10:g.160851618_160851619insGTG , CM000663.1:g.160851618_160851619insGTG | GRCh37 |
NC_000001.9:g.159118242_159118243insGTG | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326245.4:c.405+128_405+129insCAC MANE Select | ENSP00000323587.3:n.405+128_405+129insCAC | |
ENST00000326245.3:c.405+128_405+129insCAC | ENSP00000323587.3:n.405+128_405+129insCAC | |
ENST00000464077.1:n.339+128_339+129insCAC | ||
NM_017625.2:c.405+128_405+129insCAC | NP_060095.2:n.405+128_405+129insCAC | |
NM_017625.3:c.405+128_405+129insCAC MANE Select | NP_060095.2:n.405+128_405+129insCAC |