HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148994592_148994600delinsGTGGTTAGA , CM000667.2:g.148994592_148994600delinsGTGGTTAGA | GRCh38 |
NC_000005.9:g.148374155_148374163delinsGTGGTTAGA , CM000667.1:g.148374155_148374163delinsGTGGTTAGA | GRCh37 |
NC_000005.8:g.148354348_148354356delinsGTGGTTAGA | NCBI36 |
NG_007947.2:g.73575_73583delinsTCTAACCAC , LRG_269:g.73575_73583delinsTCTAACCAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515425.6:c.*10111_*10119delinsTCTAACCAC MANE Select | ENSP00000423660.1:n.*10111_*10119delinsTCTAACCAC | |
ENST00000504690.5:c.*12+9126_*12+9134delinsTCTAACCAC | ENSP00000425627.1:n.*12+9126_*12+9134delinsTCTAACCAC | |
ENST00000510350.1:n.231+12281_231+12289delinsTCTAACCAC | ||
NM_024577.3:c.*10111_*10119delinsTCTAACCAC , LRG_269t1:c.*10111_*10119delinsTCTAACCAC | NP_078853.2:n.*10111_*10119delinsTCTAACCAC | |
NM_024577.4:c.*10111_*10119delinsTCTAACCAC MANE Select | NP_078853.2:n.*10111_*10119delinsTCTAACCAC |