HGVS | Genome Assembly |
---|---|
NC_000005.10:g.10286357_10286361delinsAGACG , CM000667.2:g.10286357_10286361delinsAGACG | GRCh38 |
NC_000005.9:g.10286469_10286473delinsAGACG , CM000667.1:g.10286469_10286473delinsAGACG | GRCh37 |
NC_000005.8:g.10339469_10339473delinsAGACG | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000296658.4:c.459_463delinsCGTCT MANE Select | ENSP00000296658.3:p.Ser153= | |
ENST00000296658.3:c.459_463delinsCGTCT | ENSP00000296658.3:p.Ser153= | |
ENST00000506821.1:n.713_717delinsCGTCT | ||
ENST00000510532.5:n.527_531delinsCGTCT | ||
ENST00000511963.5:n.567_571delinsCGTCT | ||
NM_138809.3:c.459_463delinsCGTCT | NP_620164.1:p.Ser153= | |
NM_138809.4:c.459_463delinsCGTCT MANE Select | NP_620164.1:p.Ser153= |