HGVS | Genome Assembly |
---|---|
NC_000017.11:g.63942265_63942266insGGTG , CM000679.2:g.63942265_63942266insGGTG | GRCh38 |
NC_000017.10:g.62019625_62019626insGGTG , CM000679.1:g.62019625_62019626insGGTG | GRCh37 |
NC_000017.9:g.59373357_59373358insGGTG | NCBI36 |
NG_011699.1:g.35656_35657insCCAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000435607.3:c.4289-270_4289-269insCCAC MANE Select | ENSP00000396320.1:n.4289-270_4289-269insCCAC | |
ENST00000578147.5:c.4289-270_4289-269insCCAC | ENSP00000463963.1:n.4289-270_4289-269insCCAC | |
NM_000334.4:c.4289-270_4289-269insCCAC MANE Select | NP_000325.4:n.4289-270_4289-269insCCAC | |
XM_005257566.3:c.4289-270_4289-269insCCAC | XP_005257623.1:n.4289-270_4289-269insCCAC |