HGVS | Genome Assembly |
---|---|
NC_000006.12:g.3225651_3225653del , CM000668.2:g.3225651_3225653del | GRCh38 |
NC_000006.11:g.3225885_3225887del , CM000668.1:g.3225885_3225887del | GRCh37 |
NC_000006.10:g.3170884_3170886del | NCBI36 |
NG_016715.1:g.7082_7084del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000259818.8:c.436_438del MANE Select | ENSP00000259818.6:p.Gly146del | |
ENST00000680070.1:n.1366_1368del | ||
ENST00000681707.1:n.1263_1265del | ||
ENST00000681757.1:n.741_743del | ||
ENST00000259818.7:c.436_438del | ENSP00000259818.6:p.Gly146del | |
ENST00000473006.1:n.553_555del | ||
NM_178012.4:c.436_438del | NP_821080.1:p.Gly146del | |
XM_011514571.1:c.220_222del | XP_011512873.1:p.Gly74del | |
NM_178012.5:c.436_438del MANE Select | NP_821080.1:p.Gly146del |