HGVS | Genome Assembly |
---|---|
NC_000020.11:g.3082664_3082670del , CM000682.2:g.3082664_3082670del | GRCh38 |
NC_000020.10:g.3063310_3063316del , CM000682.1:g.3063310_3063316del | GRCh37 |
NC_000020.9:g.3011310_3011316del | NCBI36 |
NG_008663.1:g.7055_7061del , LRG_715:g.7055_7061del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380293.3:c.455_461del MANE Select | ENSP00000369647.3:p.Ala152GlyfsTer? | |
NM_000490.4:c.455_461del , LRG_715t1:c.455_461del | NP_000481.2:p.Ala152GlyfsTer? | |
XM_011529267.1:c.455_461del | XP_011527569.1:p.Ala152GlyfsTer? | |
XM_011529267.2:c.455_461del | XP_011527569.1:p.Ala152GlyfsTer? | |
NM_000490.5:c.455_461del MANE Select | NP_000481.2:p.Ala152GlyfsTer? |