HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94015762_94015774del , CM000663.2:g.94015762_94015774del | GRCh38 |
NC_000001.10:g.94481318_94481330del , CM000663.1:g.94481318_94481330del | GRCh37 |
NC_000001.9:g.94253906_94253918del | NCBI36 |
NG_009073.1:g.110376_110388del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.5277_5289del MANE Select | ENSP00000359245.3:p.Asn1759LysfsTer15 | |
ENST00000370225.3:c.5277_5289del | ENSP00000359245.3:p.Asn1759LysfsTer15 | |
ENST00000536513.5:c.1653_1665del | ENSP00000439707.2:p.Asn551LysfsTer15 | |
NM_000350.2:c.5277_5289del | NP_000341.2:p.Asn1759LysfsTer15 | |
NM_000350.3:c.5277_5289del MANE Select | NP_000341.2:p.Asn1759LysfsTer15 |