HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148994625_148994626del , CM000667.2:g.148994625_148994626del | GRCh38 |
NC_000005.9:g.148374188_148374189del , CM000667.1:g.148374188_148374189del | GRCh37 |
NC_000005.8:g.148354381_148354382del | NCBI36 |
NG_007947.2:g.73549_73550del , LRG_269:g.73549_73550del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515425.6:c.*10085_*10086del MANE Select | ENSP00000423660.1:n.*10085_*10086del | |
ENST00000504690.5:c.*12+9100_*12+9101del | ENSP00000425627.1:n.*12+9100_*12+9101del | |
ENST00000510350.1:n.231+12255_231+12256del | ||
NM_024577.3:c.*10085_*10086del , LRG_269t1:c.*10085_*10086del | NP_078853.2:n.*10085_*10086del | |
NM_024577.4:c.*10085_*10086del MANE Select | NP_078853.2:n.*10085_*10086del |