HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74749506_74749513delinsATGTTGGG , CM000677.2:g.74749506_74749513delinsATGTTGGG | GRCh38 |
NC_000015.9:g.75041847_75041854delinsATGTTGGG , CM000677.1:g.75041847_75041854delinsATGTTGGG | GRCh37 |
NC_000015.8:g.72828900_72828907delinsATGTTGGG | NCBI36 |
NG_008431.1:g.31965_31972delinsATGTTGGG | |
NG_008431.2:g.31965_31972delinsATGTTGGG | |
NG_061543.1:g.5662_5669delinsATGTTGGG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000343932.5:c.-9-224_-9-217delinsATGTTGGG MANE Select | ENSP00000342007.4:n.-9-224_-9-217delinsAT... | |
ENST00000343932.4:c.-9-224_-9-217delinsATGTTGGG | ENSP00000342007.4:n.-9-224_-9-217delinsAT... | |
NM_000761.4:c.-9-224_-9-217delinsATGTTGGG | NP_000752.2:n.-9-224_-9-217delinsATGTTGGG... | |
NM_000761.5:c.-9-224_-9-217delinsATGTTGGG MANE Select | NP_000752.2:n.-9-224_-9-217delinsATGTTGGG... |