HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226962_5226968delinsGTTCACC , CM000673.2:g.5226962_5226968delinsGTTCACC | GRCh38 |
NC_000011.9:g.5248192_5248198delinsGTTCACC , CM000673.1:g.5248192_5248198delinsGTTCACC | GRCh37 |
NC_000011.8:g.5204768_5204774delinsGTTCACC | NCBI36 |
NG_000007.3:g.70648_70654delinsGGTGAAC | |
NG_059281.1:g.5104_5110delinsGGTGAAC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.54_60delinsGGTGAAC | ENSP00000494175.1:p.Lys18= | |
ENST00000335295.4:c.54_60delinsGGTGAAC MANE Select | ENSP00000333994.3:p.Lys18= | |
ENST00000380315.2:c.54_60delinsGGTGAAC | ENSP00000369671.2:p.Lys18= | |
ENST00000485743.1:n.105_111delinsGGTGAAC | ||
ENST00000633227.1:c.54_60delinsGGTGAAC | ENSP00000488004.1:p.Lys18= | |
NM_000518.4:c.54_60delinsGGTGAAC | NP_000509.1:p.Lys18= | |
NM_000518.5:c.54_60delinsGGTGAAC MANE Select | NP_000509.1:p.Lys18= |