HGVS | Genome Assembly |
---|---|
NC_000016.10:g.89919988_89919992delinsACCAT , CM000678.2:g.89919988_89919992delinsACCAT | GRCh38 |
NC_000016.9:g.89986396_89986400delinsACCAT , CM000678.1:g.89986396_89986400delinsACCAT | GRCh37 |
NC_000016.8:g.88513897_88513901delinsACCAT | NCBI36 |
NG_012026.1:g.7110_7114delinsACCAT | |
NG_027810.1:g.2980_2984delinsACCAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000555147.2:c.730_734delinsACCAT MANE Select | ENSP00000451605.1:p.Thr244= | |
ENST00000639847.1:c.730_734delinsACCAT | ENSP00000492011.1:p.Thr244= | |
ENST00000555147.1:c.730_734delinsACCAT | ENSP00000451605.1:p.Thr244= | |
ENST00000555427.1:c.730_734delinsACCAT | ENSP00000451760.1:p.Thr244= | |
ENST00000556922.1:c.730_734delinsACCAT | ENSP00000451560.1:p.Thr244= | |
NM_002386.3:c.730_734delinsACCAT | NP_002377.4:p.Thr244= | |
NM_002386.4:c.730_734delinsACCAT MANE Select | NP_002377.4:p.Thr244= |