HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31270008_31270009insT , CM000668.2:g.31270008_31270009insT | GRCh38 |
NC_000006.11:g.31237785_31237786insT , CM000668.1:g.31237785_31237786insT | GRCh37 |
NC_000006.10:g.31345764_31345765insT | NCBI36 |
NG_029422.2:g.7123_7124insA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000376228.10:c.972_973insA MANE Select | ENSP00000365402.5:p.Gly325ArgfsTer10 | |
ENST00000376228.9:c.972_973insA | ENSP00000365402.5:p.Gly325ArgfsTer10 | |
ENST00000376237.8:c.*559_*560insA | ENSP00000365412.4:n.*559_*560insA | |
ENST00000383329.7:c.972_973insA | ENSP00000372819.3:p.Gly325ArgfsTer10 | |
ENST00000470363.5:n.290_291insA | ||
ENST00000487245.5:n.1331_1332insA | ||
NM_002117.5:c.972_973insA | NP_002108.4:p.Gly325ArgfsTer10 | |
NM_002117.6:c.972_973insA MANE Select | NP_002108.4:p.Gly325ArgfsTer10 |