HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571687_154571689del , CM000663.2:g.154571687_154571689del | GRCh38 |
NC_000001.10:g.154544163_154544165del , CM000663.1:g.154544163_154544165del | GRCh37 |
NC_000001.9:g.152810787_152810789del | NCBI36 |
NG_008027.1:g.8907_8909del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.864_866del MANE Select | ENSP00000357461.3:p.Pro289del | |
ENST00000636034.1:c.864_866del | ENSP00000489703.1:p.Pro289del | |
ENST00000637900.1:c.870_872del | ENSP00000490474.1:p.Pro291del | |
ENST00000368476.3:c.864_866del | ENSP00000357461.3:p.Pro289del | |
NM_000748.2:c.864_866del | NP_000739.1:p.Pro289del | |
XM_017000180.2:c.354_356del | XP_016855669.1:p.Pro119del | |
XR_001736952.2:n.1116_1118del | ||
NM_000748.3:c.864_866del MANE Select | NP_000739.1:p.Pro289del |