HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226781_5226782delinsAG , CM000673.2:g.5226781_5226782delinsAG | GRCh38 |
NC_000011.9:g.5248011_5248012delinsAG , CM000673.1:g.5248011_5248012delinsAG | GRCh37 |
NC_000011.8:g.5204587_5204588delinsAG | NCBI36 |
NG_000007.3:g.70834_70835delinsCT | |
NG_059281.1:g.5290_5291delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647020.1:c.110_111delinsCT | ENSP00000494175.1:p.Pro37= | |
ENST00000335295.4:c.110_111delinsCT MANE Select | ENSP00000333994.3:p.Pro37= | |
ENST00000380315.2:c.110_111delinsCT | ENSP00000369671.2:p.Pro37= | |
ENST00000475226.1:n.42_43delinsCT | ||
ENST00000485743.1:n.161_162delinsCT | ||
ENST00000633227.1:c.94_95delinsCT | ENSP00000488004.1:p.Leu32= | |
NM_000518.4:c.110_111delinsCT | NP_000509.1:p.Pro37= | |
NM_000518.5:c.110_111delinsCT MANE Select | NP_000509.1:p.Pro37= |