HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226975_5226978del , CM000673.2:g.5226975_5226978del | GRCh38 |
NC_000011.9:g.5248205_5248208del , CM000673.1:g.5248205_5248208del | GRCh37 |
NC_000011.8:g.5204781_5204784del | NCBI36 |
NG_000007.3:g.70638_70641del | |
NG_059281.1:g.5094_5097del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.44_47del | ENSP00000494175.1:p.Leu15ArgfsTer4 | |
ENST00000335295.4:c.44_47del MANE Select | ENSP00000333994.3:p.Leu15ArgfsTer4 | |
ENST00000380315.2:c.44_47del | ENSP00000369671.2:p.Leu15ArgfsTer4 | |
ENST00000485743.1:n.95_98del | ||
ENST00000633227.1:c.44_47del | ENSP00000488004.1:p.Leu15ArgfsTer4 | |
NM_000518.4:c.44_47del | NP_000509.1:p.Leu15ArgfsTer4 | |
NM_000518.5:c.44_47del MANE Select | NP_000509.1:p.Leu15ArgfsTer4 |