HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226930_5226931delinsCT , CM000673.2:g.5226930_5226931delinsCT | GRCh38 |
NC_000011.9:g.5248160_5248161delinsCT , CM000673.1:g.5248160_5248161delinsCT | GRCh37 |
NC_000011.8:g.5204736_5204737delinsCT | NCBI36 |
NG_000007.3:g.70685_70686delinsAG | |
NG_059281.1:g.5141_5142delinsAG |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.91_92delinsAG | ENSP00000494175.1:p.Arg31= | |
ENST00000335295.4:c.91_92delinsAG MANE Select | ENSP00000333994.3:p.Arg31= | |
ENST00000380315.2:c.91_92delinsAG | ENSP00000369671.2:p.Arg31= | |
ENST00000485743.1:n.142_143delinsAG | ||
ENST00000633227.1:c.76+15_76+16delinsAG | ENSP00000488004.1:n.76+15_76+16delinsAG | |
NM_000518.4:c.91_92delinsAG | NP_000509.1:p.Arg31= | |
NM_000518.5:c.91_92delinsAG MANE Select | NP_000509.1:p.Arg31= |