HGVS | Genome Assembly |
---|---|
NC_000005.10:g.159315982_159315990del , CM000667.2:g.159315982_159315990del | GRCh38 |
NC_000005.9:g.158742990_158742998del , CM000667.1:g.158742990_158742998del | GRCh37 |
NC_000005.8:g.158675568_158675576del | NCBI36 |
NG_009618.1:g.19484_19492del , LRG_71:g.19484_19492del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696750.1:c.*111_*119del | ENSP00000512849.1:n.*111_*119del | |
ENST00000696751.1:c.*593_*601del | ENSP00000512850.1:n.*593_*601del | |
ENST00000231228.3:c.*111_*119del MANE Select | ENSP00000231228.2:n.*111_*119del | |
ENST00000231228.2:c.*111_*119del | ENSP00000231228.2:n.*111_*119del | |
NM_002187.2:c.*111_*119del , LRG_71t1:c.*111_*119del | NP_002178.2:n.*111_*119del | |
NM_002187.3:c.*111_*119del MANE Select | NP_002178.2:n.*111_*119del |