HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94029591_94029604del , CM000663.2:g.94029591_94029604del | GRCh38 |
NC_000001.10:g.94495147_94495160del , CM000663.1:g.94495147_94495160del | GRCh37 |
NC_000001.9:g.94267735_94267748del | NCBI36 |
NG_009073.1:g.96549_96562del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.4383_4396del MANE Select | ENSP00000359245.3:p.Trp1461CysfsTer? | |
ENST00000370225.3:c.4383_4396del | ENSP00000359245.3:p.Trp1461CysfsTer? | |
ENST00000536513.5:c.759_772del | ENSP00000439707.2:p.Trp253CysfsTer? | |
NM_000350.2:c.4383_4396del | NP_000341.2:p.Trp1461CysfsTer? | |
NM_000350.3:c.4383_4396del MANE Select | NP_000341.2:p.Trp1461CysfsTer? |