HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94775413_94775416del , CM000672.2:g.94775413_94775416del | GRCh38 |
NC_000010.10:g.96535170_96535173del , CM000672.1:g.96535170_96535173del | GRCh37 |
NC_000010.9:g.96525160_96525163del | NCBI36 |
NG_008384.2:g.17708_17711del | |
NG_008384.3:g.17733_17736del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.355_358del MANE Select | ENSP00000360372.3:p.Arg119GlyfsTer10 | |
ENST00000645461.1:n.1408_1411del | ||
ENST00000371321.7:c.355_358del | ENSP00000360372.3:p.Arg119GlyfsTer10 | |
ENST00000464755.1:c.1118_1121del | ENSP00000483243.1:n.1118_1121del | |
ENST00000480405.2:c.355_358del | ENSP00000483847.1:p.Arg119GlyfsTer10 | |
NM_000769.2:c.355_358del | NP_000760.1:p.Arg119GlyfsTer10 | |
NM_000769.4:c.355_358del MANE Select | NP_000760.1:p.Arg119GlyfsTer10 |