HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43551490_43551491delinsAG , CM000681.2:g.43551490_43551491delinsAG | GRCh38 |
NC_000019.9:g.44055642_44055643delinsAG , CM000681.1:g.44055642_44055643delinsAG | GRCh37 |
NC_000019.8:g.48747482_48747483delinsAG | NCBI36 |
NG_033799.1:g.29088_29089delinsCT , LRG_784:g.29088_29089delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000262887.10:c.1199+80_1199+81delinsCT MANE Select | ENSP00000262887.5:n.1199+80_1199+81delins... | |
ENST00000262887.9:c.1199+80_1199+81delinsCT | ENSP00000262887.4:n.1199+80_1199+81delins... | |
ENST00000543982.5:c.1106+80_1106+81delinsCT | ENSP00000443671.1:n.1106+80_1106+81delins... | |
NM_006297.2:c.1199+80_1199+81delinsCT , LRG_784t1:c.1199+80_1199+81delinsCT | NP_006288.2:n.1199+80_1199+81delinsCT | |
NM_006297.3:c.1199+80_1199+81delinsCT MANE Select | NP_006288.2:n.1199+80_1199+81delinsCT |