HGVS | Genome Assembly |
---|---|
NC_000001.11:g.154571685_154571686insA , CM000663.2:g.154571685_154571686insA | GRCh38 |
NC_000001.10:g.154544161_154544162insA , CM000663.1:g.154544161_154544162insA | GRCh37 |
NC_000001.9:g.152810785_152810786insA | NCBI36 |
NG_008027.1:g.8905_8906insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368476.4:c.862_863insA MANE Select | ENSP00000357461.3:p.Pro288HisfsTer? | |
ENST00000636034.1:c.862_863insA | ENSP00000489703.1:p.Pro288HisfsTer? | |
ENST00000637900.1:c.868_869insA | ENSP00000490474.1:p.Pro290HisfsTer? | |
ENST00000368476.3:c.862_863insA | ENSP00000357461.3:p.Pro288HisfsTer? | |
NM_000748.2:c.862_863insA | NP_000739.1:p.Pro288HisfsTer? | |
XM_017000180.2:c.352_353insA | XP_016855669.1:p.Pro118HisfsTer? | |
XR_001736952.2:n.1114_1115insA | ||
NM_000748.3:c.862_863insA MANE Select | NP_000739.1:p.Pro288HisfsTer? |