HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226797_5226798delinsAG , CM000673.2:g.5226797_5226798delinsAG | GRCh38 |
NC_000011.9:g.5248027_5248028delinsAG , CM000673.1:g.5248027_5248028delinsAG | GRCh37 |
NC_000011.8:g.5204603_5204604delinsAG | NCBI36 |
NG_000007.3:g.70818_70819delinsCT | |
NG_059281.1:g.5274_5275delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647020.1:c.94_95delinsCT | ENSP00000494175.1:p.Leu32= | |
ENST00000335295.4:c.94_95delinsCT MANE Select | ENSP00000333994.3:p.Leu32= | |
ENST00000380315.2:c.94_95delinsCT | ENSP00000369671.2:p.Leu32= | |
ENST00000475226.1:n.26_27delinsCT | ||
ENST00000485743.1:n.145_146delinsCT | ||
ENST00000633227.1:c.78_79delinsCT | ENSP00000488004.1:p.Gly26= | |
NM_000518.4:c.94_95delinsCT | NP_000509.1:p.Leu32= | |
NM_000518.5:c.94_95delinsCT MANE Select | NP_000509.1:p.Leu32= |