HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149884703_149884707del , CM000663.2:g.149884703_149884707del | GRCh38 |
NC_000001.10:g.149856253_149856257del , CM000663.1:g.149856253_149856257del | GRCh37 |
NC_000001.9:g.148122877_148122881del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369155.4:c.*1553_*1557del MANE Select | ENSP00000358151.2:n.*1553_*1557del | |
ENST00000369155.3:c.*1553_*1557del | ENSP00000358151.2:n.*1553_*1557del | |
ENST00000369160.3:c.377+1557_377+1561del | ENSP00000375736.2:n.377+1557_377+1561del | |
NM_003528.2:c.*1553_*1557del | NP_003519.1:n.*1553_*1557del | |
NM_003528.3:c.*1553_*1557del MANE Select | NP_003519.1:n.*1553_*1557del |