HGVS | Genome Assembly |
---|---|
NC_000001.11:g.193251440_193251441del , CM000663.2:g.193251440_193251441del | GRCh38 |
NC_000001.10:g.193220570_193220571del , CM000663.1:g.193220570_193220571del | GRCh37 |
NC_000001.9:g.191487193_191487194del | NCBI36 |
NG_012691.1:g.134483_134484del , LRG_507:g.134483_134484del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000367435.5:c.*728_*729del MANE Select | ENSP00000356405.4:n.*728_*729del | |
ENST00000635846.1:c.*728_*729del | ENSP00000490035.1:n.*728_*729del | |
ENST00000643006.1:c.*1234_*1235del | ENSP00000496633.1:n.*1234_*1235del | |
ENST00000367435.3:c.*728_*729del | ENSP00000356405.3:n.*728_*729del | |
NM_024529.4:c.*728_*729del , LRG_507t1:c.*728_*729del | NP_078805.3:n.*728_*729del | |
NM_024529.5:c.*728_*729del MANE Select | NP_078805.3:n.*728_*729del |