HGVS | Genome Assembly |
---|---|
NC_000011.10:g.124873050_124873051del , CM000673.2:g.124873050_124873051del | GRCh38 |
NC_000011.9:g.124742946_124742947del , CM000673.1:g.124742946_124742947del | GRCh37 |
NC_000011.8:g.124248156_124248157del | NCBI36 |
NG_016214.1:g.12642_12643del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000397801.6:c.1497_1498del MANE Select | ENSP00000380903.1:p.Lys499AsnfsTer? | |
ENST00000397801.5:c.1497_1498del | ENSP00000380903.1:p.Lys499AsnfsTer? | |
ENST00000538940.5:c.1431_1432del | ENSP00000441797.1:p.Lys477AsnfsTer? | |
NM_022370.3:c.1497_1498del | NP_071765.2:p.Lys499AsnfsTer? | |
XM_011542953.1:c.2469_2470del | XP_011541255.1:p.Lys823AsnfsTer? | |
XM_017018122.1:c.1431_1432del | XP_016873611.1:p.Lys477AsnfsTer? | |
NM_022370.4:c.1497_1498del MANE Select | NP_071765.2:p.Lys499AsnfsTer? |