HGVS | Genome Assembly |
---|---|
NC_000017.11:g.70175756_70175757delinsAG , CM000679.2:g.70175756_70175757delinsAG | GRCh38 |
NC_000017.10:g.68171897_68171898delinsAG , CM000679.1:g.68171897_68171898delinsAG | GRCh37 |
NC_000017.9:g.65683492_65683493delinsAG | NCBI36 |
NG_008798.1:g.11222_11223delinsAG , LRG_328:g.11222_11223delinsAG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000243457.4:c.717_718delinsAG MANE Select | ENSP00000243457.2:p.Glu239= | |
ENST00000243457.3:c.717_718delinsAG | ENSP00000243457.2:p.Glu239= | |
ENST00000535240.1:c.717_718delinsAG | ENSP00000441848.1:p.Glu239= | |
NM_000891.2:c.717_718delinsAG , LRG_328t1:c.717_718delinsAG | NP_000882.1:p.Glu239= | |
XM_011524779.1:c.717_718delinsAG | XP_011523081.1:p.Glu239= | |
NM_000891.3:c.717_718delinsAG MANE Select | NP_000882.1:p.Glu239= |