HGVS | Genome Assembly |
---|---|
NC_000010.11:g.110812366_110812367delinsAT , CM000672.2:g.110812366_110812367delinsAT | GRCh38 |
NC_000010.10:g.112572124_112572125delinsAT , CM000672.1:g.112572124_112572125delinsAT | GRCh37 |
NC_000010.9:g.112562114_112562115delinsAT | NCBI36 |
NG_021177.1:g.172970_172971delinsAT , LRG_382:g.172970_172971delinsAT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369519.4:c.1969_1970delinsAT MANE Select | ENSP00000358532.3:p.Ser657Ile | |
ENST00000369519.3:c.1969_1970delinsAT | ENSP00000358532.3:p.Ser657Ile | |
NM_001134363.2:c.1969_1970delinsAT | NP_001127835.2:p.Ser657Ile | |
XM_011539697.1:c.1585_1586delinsAT | XP_011537999.1:p.Ser529Ile | |
XM_017016103.2:c.1804_1805delinsAT | XP_016871592.1:p.Ser602Ile | |
XM_017016104.2:c.1585_1586delinsAT | XP_016871593.1:p.Ser529Ile | |
NM_001134363.3:c.1969_1970delinsAT MANE Select | NP_001127835.2:p.Ser657Ile |