HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5226624_5226626delinsTCA , CM000673.2:g.5226624_5226626delinsTCA | GRCh38 |
NC_000011.9:g.5247854_5247856delinsTCA , CM000673.1:g.5247854_5247856delinsTCA | GRCh37 |
NC_000011.8:g.5204430_5204432delinsTCA | NCBI36 |
NG_000007.3:g.70990_70992delinsTGA | |
NG_059281.1:g.5446_5448delinsTGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000647020.1:c.266_268delinsTGA | ENSP00000494175.1:p.Leu89= | |
ENST00000335295.4:c.266_268delinsTGA MANE Select | ENSP00000333994.3:p.Leu89= | |
ENST00000380315.2:c.266_268delinsTGA | ENSP00000369671.2:p.Leu89= | |
ENST00000475226.1:n.198_200delinsTGA | ||
ENST00000485743.1:n.317_319delinsTGA | ||
ENST00000633227.1:c.*82_*84delinsTGA | ENSP00000488004.1:n.*82_*84delinsTGA | |
NM_000518.4:c.266_268delinsTGA | NP_000509.1:p.Leu89= | |
NM_000518.5:c.266_268delinsTGA MANE Select | NP_000509.1:p.Leu89= |