HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94021499_94021500insACAC , CM000663.2:g.94021499_94021500insACAC | GRCh38 |
NC_000001.10:g.94487055_94487056insACAC , CM000663.1:g.94487055_94487056insACAC | GRCh37 |
NC_000001.9:g.94259643_94259644insACAC | NCBI36 |
NG_009073.1:g.104650_104651insGTGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.4849-91_4849-90insGTGT MANE Select | ENSP00000359245.3:n.4849-91_4849-90insGTGT | |
ENST00000370225.3:c.4849-91_4849-90insGTGT | ENSP00000359245.3:n.4849-91_4849-90insGTGT | |
ENST00000460514.1:n.343-91_343-90insGTGT | ||
ENST00000536513.5:c.1225-91_1225-90insGTGT | ENSP00000439707.2:n.1225-91_1225-90insGTGT | |
NM_000350.2:c.4849-91_4849-90insGTGT | NP_000341.2:n.4849-91_4849-90insGTGT | |
NM_000350.3:c.4849-91_4849-90insGTGT MANE Select | NP_000341.2:n.4849-91_4849-90insGTGT |