HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148994637_148994638delinsTG , CM000667.2:g.148994637_148994638delinsTG | GRCh38 |
NC_000005.9:g.148374200_148374201delinsTG , CM000667.1:g.148374200_148374201delinsTG | GRCh37 |
NC_000005.8:g.148354393_148354394delinsTG | NCBI36 |
NG_007947.2:g.73537_73538delinsCA , LRG_269:g.73537_73538delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515425.6:c.*10073_*10074delinsCA MANE Select | ENSP00000423660.1:n.*10073_*10074delinsCA | |
ENST00000504690.5:c.*12+9088_*12+9089delinsCA | ENSP00000425627.1:n.*12+9088_*12+9089delinsCA | |
ENST00000510350.1:n.231+12243_231+12244delinsCA | ||
NM_024577.3:c.*10073_*10074delinsCA , LRG_269t1:c.*10073_*10074delinsCA | NP_078853.2:n.*10073_*10074delinsCA | |
NM_024577.4:c.*10073_*10074delinsCA MANE Select | NP_078853.2:n.*10073_*10074delinsCA |