HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154966080_154966082delinsA , CM000685.2:g.154966080_154966082delinsA | GRCh38 |
NC_000023.10:g.154194355_154194357delinsA , CM000685.1:g.154194355_154194357delinsA | GRCh37 |
NC_000023.9:g.153847549_153847551delinsA | NCBI36 |
NG_011403.1:g.61642_61644delinsT | |
NG_011403.2:g.61642_61644delinsT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.1331_1333delinsT MANE Select | ENSP00000353393.4:p.Lys444IlefsTer9 | |
ENST00000647125.1:c.*1207_*1209delinsT | ENSP00000496062.1:n.*1207_*1209delinsT | |
ENST00000360256.8:c.1331_1333delinsT | ENSP00000353393.4:p.Lys444IlefsTer9 | |
ENST00000483822.2:n.151_153delinsT | ||
NM_000132.3:c.1331_1333delinsT | NP_000123.1:p.Lys444IlefsTer9 | |
XM_011531126.1:c.1226_1228delinsT | XP_011529428.1:p.Lys409IlefsTer9 | |
NM_000132.4:c.1331_1333delinsT MANE Select | NP_000123.1:p.Lys444IlefsTer9 |