HGVS | Genome Assembly |
---|---|
NC_000012.12:g.12717815_12717816delinsGC , CM000674.2:g.12717815_12717816delinsGC | GRCh38 |
NC_000012.11:g.12870749_12870750delinsGC , CM000674.1:g.12870749_12870750delinsGC | GRCh37 |
NC_000012.10:g.12762016_12762017delinsGC | NCBI36 |
NG_016341.1:g.5448_5449delinsGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000614874.2:c.-25_-24delinsGC | ENSP00000507272.1:n.-25_-24delinsGC | |
ENST00000682620.1:n.1631-1010_1631-1009delinsGC | ||
ENST00000684771.1:n.585-1010_585-1009delinsGC | ||
ENST00000228872.9:c.-25_-24delinsGC MANE Select | ENSP00000228872.4:n.-25_-24delinsGC | |
ENST00000228872.8:c.-25_-24delinsGC | ENSP00000228872.4:n.-25_-24delinsGC | |
ENST00000477087.1:n.155-1010_155-1009delinsGC | ||
NM_004064.4:c.-25_-24delinsGC | NP_004055.1:n.-25_-24delinsGC | |
NM_004064.5:c.-25_-24delinsGC MANE Select | NP_004055.1:n.-25_-24delinsGC |