HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226942_5226943insA , CM000673.2:g.5226942_5226943insA | GRCh38 |
NC_000011.9:g.5248172_5248173insA , CM000673.1:g.5248172_5248173insA | GRCh37 |
NC_000011.8:g.5204748_5204749insA | NCBI36 |
NG_000007.3:g.70673_70674insT | |
NG_059281.1:g.5129_5130insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647020.1:c.79_80insT | ENSP00000494175.1:p.Glu27ValfsTer18 | |
ENST00000335295.4:c.79_80insT MANE Select | ENSP00000333994.3:p.Glu27ValfsTer18 | |
ENST00000380315.2:c.79_80insT | ENSP00000369671.2:p.Glu27ValfsTer18 | |
ENST00000485743.1:n.130_131insT | ||
ENST00000633227.1:c.76+3_76+4insT | ENSP00000488004.1:n.76+3_76+4insT | |
NM_000518.4:c.79_80insT | NP_000509.1:p.Glu27ValfsTer18 | |
NM_000518.5:c.79_80insT MANE Select | NP_000509.1:p.Glu27ValfsTer18 |