HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149884718_149884720del , CM000663.2:g.149884718_149884720del | GRCh38 |
NC_000001.10:g.149856268_149856270del , CM000663.1:g.149856268_149856270del | GRCh37 |
NC_000001.9:g.148122892_148122894del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369155.4:c.*1541_*1543del MANE Select | ENSP00000358151.2:n.*1541_*1543del | |
ENST00000369155.3:c.*1541_*1543del | ENSP00000358151.2:n.*1541_*1543del | |
ENST00000369160.3:c.377+1545_377+1547del | ENSP00000375736.2:n.377+1545_377+1547del | |
NM_003528.2:c.*1541_*1543del | NP_003519.1:n.*1541_*1543del | |
NM_003528.3:c.*1541_*1543del MANE Select | NP_003519.1:n.*1541_*1543del |