HGVS | Genome Assembly |
---|---|
NC_000023.11:g.47574185_47574188delinsGGGC , CM000685.2:g.47574185_47574188delinsGGGC | GRCh38 |
NC_000023.10:g.47433584_47433587delinsGGGC , CM000685.1:g.47433584_47433587delinsGGGC | GRCh37 |
NC_000023.9:g.47318528_47318531delinsGGGC | NCBI36 |
NG_008437.1:g.50670_50673delinsGCCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295987.13:c.1796_1799delinsGCCC MANE Select | ENSP00000295987.7:p.Gly599= | |
ENST00000340666.5:c.1796_1799delinsGCCC | ENSP00000343206.4:p.Gly599= | |
ENST00000640721.1:c.70+500_70+503delinsGCCC | ENSP00000492857.1:n.70+500_70+503delinsGCCC | |
ENST00000295987.11:c.1796_1799delinsGCCC | ENSP00000295987.7:p.Gly599= | |
ENST00000340666.4:c.1796_1799delinsGCCC | ENSP00000343206.4:p.Gly599= | |
NM_006950.3:c.1796_1799delinsGCCC MANE Select | NP_008881.2:p.Gly599= | |
NM_133499.2:c.1796_1799delinsGCCC | NP_598006.1:p.Gly599= |