HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571688_154571690del , CM000663.2:g.154571688_154571690del | GRCh38 |
NC_000001.10:g.154544164_154544166del , CM000663.1:g.154544164_154544166del | GRCh37 |
NC_000001.9:g.152810788_152810790del | NCBI36 |
NG_008027.1:g.8908_8910del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.865_867del MANE Select | ENSP00000357461.3:p.Pro289del | |
ENST00000636034.1:c.865_867del | ENSP00000489703.1:p.Pro289del | |
ENST00000637900.1:c.871_873del | ENSP00000490474.1:p.Pro291del | |
ENST00000368476.3:c.865_867del | ENSP00000357461.3:p.Pro289del | |
NM_000748.2:c.865_867del | NP_000739.1:p.Pro289del | |
XM_017000180.2:c.355_357del | XP_016855669.1:p.Pro119del | |
XR_001736952.2:n.1117_1119del | ||
NM_000748.3:c.865_867del MANE Select | NP_000739.1:p.Pro289del |