HGVS | Genome Assembly |
---|---|
NC_000021.9:g.46001274_46001277delinsACCT , CM000683.2:g.46001274_46001277delinsACCT | GRCh38 |
NC_000021.8:g.47421188_47421191delinsACCT , CM000683.1:g.47421188_47421191delinsACCT | GRCh37 |
NC_000021.7:g.46245616_46245619delinsACCT | NCBI36 |
NG_008674.1:g.24526_24529delinsACCT , LRG_475:g.24526_24529delinsACCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000463060.6:n.243_246delinsACCT | ||
ENST00000361866.8:c.1844_1847delinsACCT MANE Select | ENSP00000355180.3:p.Asp615= | |
ENST00000361866.7:c.1844_1847delinsACCT | ENSP00000355180.3:p.Asp615= | |
ENST00000463060.5:n.243_246delinsACCT | ||
ENST00000498614.5:n.78_81delinsACCT | ||
ENST00000612273.1:c.1838_1841delinsACCT | ENSP00000483630.1:p.Asp613= | |
NM_001848.2:c.1844_1847delinsACCT , LRG_475t1:c.1844_1847delinsACCT | NP_001839.2:p.Asp615= | |
NM_001848.3:c.1844_1847delinsACCT MANE Select | NP_001839.2:p.Asp615= |