HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225622_3225623insA , CM000668.2:g.3225622_3225623insA | GRCh38 |
NC_000006.11:g.3225856_3225857insA , CM000668.1:g.3225856_3225857insA | GRCh37 |
NC_000006.10:g.3170855_3170856insA | NCBI36 |
NG_016715.1:g.7112_7113insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.466_467insT MANE Select | ENSP00000259818.6:p.Arg156LeufsTer? | |
ENST00000680070.1:n.1396_1397insT | ||
ENST00000681707.1:n.1293_1294insT | ||
ENST00000681757.1:n.771_772insT | ||
ENST00000259818.7:c.466_467insT | ENSP00000259818.6:p.Arg156LeufsTer? | |
ENST00000473006.1:n.583_584insT | ||
NM_178012.4:c.466_467insT | NP_821080.1:p.Arg156LeufsTer? | |
XM_011514571.1:c.250_251insT | XP_011512873.1:p.Arg84LeufsTer? | |
NM_178012.5:c.466_467insT MANE Select | NP_821080.1:p.Arg156LeufsTer? |