HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154154628_154154647delinsCTCGTACCCCGGGGTGCAGT , CM000685.2:g.154154628_154154647delinsCTCGTACCCCGGGGTGCAGT | GRCh38 |
NC_000023.10:g.153420103_153420122delinsCTCGTACCCCGGGGTGCAGT , CM000685.1:g.153420103_153420122delinsCTCGTACCCCGGGGTGCAGT | GRCh37 |
NC_000023.9:g.153073297_153073316delinsCTCGTACCCCGGGGTGCAGT | NCBI36 |
NG_009105.2:g.15378_15397delinsCTCGTACCCCGGGGTGCAGT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369951.9:c.633_652delinsCTCGTACCCCGGGGTGCAGT MANE Select | ENSP00000358967.4:p.Ser211= | |
ENST00000369951.8:c.633_652delinsCTCGTACCCCGGGGTGCAGT | ENSP00000358967.4:p.Ser211= | |
ENST00000442922.1:c.222_241delinsCTCGTACCCCGGGGTGCAGT | ENSP00000402493.1:p.Ser74= | |
ENST00000463296.1:n.588+1520_588+1539delinsCTCGTACCCCGGGGTGCAGT | ||
NM_020061.5:c.633_652delinsCTCGTACCCCGGGGTGCAGT | NP_064445.2:p.Ser211= | |
NM_020061.6:c.633_652delinsCTCGTACCCCGGGGTGCAGT MANE Select | NP_064445.2:p.Ser211= |