HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29070997_29070999dup , CM000664.2:g.29070997_29070999dup | GRCh38 |
NC_000002.11:g.29293863_29293865dup , CM000664.1:g.29293863_29293865dup | GRCh37 |
NC_000002.10:g.29147367_29147369dup | NCBI36 |
NG_021427.1:g.8264_8266dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.3264_3266dup MANE Select | ENSP00000332809.4:p.Pro1089_Ser1090insPro | |
ENST00000331664.5:c.3264_3266dup | ENSP00000332809.4:p.Pro1089_Ser1090insPro | |
NM_001029883.2:c.3264_3266dup | NP_001025054.1:p.Pro1089_Ser1090insPro | |
XM_011532826.1:c.3264_3266dup | XP_011531128.1:p.Pro1089_Ser1090insPro | |
XR_939901.1:n.185+1830_185+1832dup | ||
XR_939902.1:n.173+1842_173+1844dup | ||
NM_001029883.3:c.3264_3266dup MANE Select | NP_001025054.1:p.Pro1089_Ser1090insPro |