HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148994559dup , CM000667.2:g.148994559dup | GRCh38 |
NC_000005.9:g.148374122dup , CM000667.1:g.148374122dup | GRCh37 |
NC_000005.8:g.148354315dup | NCBI36 |
NG_007947.2:g.73617dup , LRG_269:g.73617dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000515425.6:c.*10153dup MANE Select | ENSP00000423660.1:n.*10153dup | |
ENST00000504690.5:c.*12+9168dup | ENSP00000425627.1:n.*12+9168dup | |
ENST00000510350.1:n.231+12323dup | ||
NM_024577.3:c.*10153dup , LRG_269t1:c.*10153dup | NP_078853.2:n.*10153dup | |
NM_024577.4:c.*10153dup MANE Select | NP_078853.2:n.*10153dup |