HGVS | Genome Assembly |
---|---|
NC_000011.10:g.124872548del , CM000673.2:g.124872548del | GRCh38 |
NC_000011.9:g.124742444del , CM000673.1:g.124742444del | GRCh37 |
NC_000011.8:g.124247654del | NCBI36 |
NG_016214.1:g.12140del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000397801.6:c.1326del MANE Select | ENSP00000380903.1:p.Gly443GlufsTer? | |
ENST00000397801.5:c.1326del | ENSP00000380903.1:p.Gly443GlufsTer? | |
ENST00000538940.5:c.1260del | ENSP00000441797.1:p.Gly421GlufsTer? | |
NM_022370.3:c.1326del | NP_071765.2:p.Gly443GlufsTer? | |
XM_011542953.1:c.2298del | XP_011541255.1:p.Gly767GlufsTer? | |
XM_017018122.1:c.1260del | XP_016873611.1:p.Gly421GlufsTer? | |
NM_022370.4:c.1326del MANE Select | NP_071765.2:p.Gly443GlufsTer? |