HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225567_3225568insAG , CM000668.2:g.3225567_3225568insAG | GRCh38 |
NC_000006.11:g.3225801_3225802insAG , CM000668.1:g.3225801_3225802insAG | GRCh37 |
NC_000006.10:g.3170800_3170801insAG | NCBI36 |
NG_016715.1:g.7167_7168insCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.521_522insCT MANE Select | ENSP00000259818.6:p.Lys174AsnfsTer? | |
ENST00000680070.1:n.1451_1452insCT | ||
ENST00000681707.1:n.1348_1349insCT | ||
ENST00000681757.1:n.826_827insCT | ||
ENST00000259818.7:c.521_522insCT | ENSP00000259818.6:p.Lys174AsnfsTer? | |
ENST00000473006.1:n.638_639insCT | ||
NM_178012.4:c.521_522insCT | NP_821080.1:p.Lys174AsnfsTer? | |
XM_011514571.1:c.305_306insCT | XP_011512873.1:p.Lys102AsnfsTer? | |
NM_178012.5:c.521_522insCT MANE Select | NP_821080.1:p.Lys174AsnfsTer? |