HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94780444_94780445insGTAAAC , CM000672.2:g.94780444_94780445insGTAAAC | GRCh38 |
NC_000010.10:g.96540201_96540202insGTAAAC , CM000672.1:g.96540201_96540202insGTAAAC | GRCh37 |
NC_000010.9:g.96530191_96530192insGTAAAC | NCBI36 |
NG_008384.2:g.22739_22740insGTAAAC | |
NG_008384.3:g.22764_22765insGTAAAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.482-55_482-54insGTAAAC MANE Select | ENSP00000360372.3:n.482-55_482-54insGTAAAC | |
ENST00000645461.1:n.1535-55_1535-54insGTAAAC | ||
ENST00000371321.7:c.482-55_482-54insGTAAAC | ENSP00000360372.3:n.482-55_482-54insGTAAAC | |
ENST00000464755.1:c.1245-55_1245-54insGTAAAC | ENSP00000483243.1:n.1245-55_1245-54insGTAAAC | |
NM_000769.2:c.482-55_482-54insGTAAAC | NP_000760.1:n.482-55_482-54insGTAAAC | |
NM_000769.4:c.482-55_482-54insGTAAAC MANE Select | NP_000760.1:n.482-55_482-54insGTAAAC |