HGVS | Genome Assembly |
---|---|
NC_000015.10:g.90501078_90501079delinsCT , CM000677.2:g.90501078_90501079delinsCT | GRCh38 |
NC_000015.9:g.91044310_91044311delinsCT , CM000677.1:g.91044310_91044311delinsCT | GRCh37 |
NC_000015.8:g.88845314_88845315delinsCT | NCBI36 |
NG_052946.1:g.117838_117839delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000268182.10:c.*970_*971delinsCT MANE Select | ENSP00000268182.5:n.*970_*971delinsCT | |
ENST00000268182.9:c.*970_*971delinsCT | ENSP00000268182.5:n.*970_*971delinsCT | |
ENST00000558957.1:n.2002_2003delinsCT | ||
ENST00000561086.1:n.1711_1712delinsCT | ||
NM_003870.3:c.*970_*971delinsCT | NP_003861.1:n.*970_*971delinsCT | |
XR_001751409.2:n.6073_6074delinsCT | ||
NM_003870.4:c.*970_*971delinsCT MANE Select | NP_003861.1:n.*970_*971delinsCT |