HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29070684_29070687delinsGTCC , CM000664.2:g.29070684_29070687delinsGTCC | GRCh38 |
NC_000002.11:g.29293550_29293553delinsGTCC , CM000664.1:g.29293550_29293553delinsGTCC | GRCh37 |
NC_000002.10:g.29147054_29147057delinsGTCC | NCBI36 |
NG_021427.1:g.8575_8578delinsGGAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.3575_3578delinsGGAC MANE Select | ENSP00000332809.4:p.Arg1192= | |
ENST00000331664.5:c.3575_3578delinsGGAC | ENSP00000332809.4:p.Arg1192= | |
NM_001029883.2:c.3575_3578delinsGGAC | NP_001025054.1:p.Arg1192= | |
XM_011532826.1:c.3575_3578delinsGGAC | XP_011531128.1:p.Arg1192= | |
XR_939901.1:n.185+1517_185+1520delinsGTCC | ||
XR_939902.1:n.173+1529_173+1532delinsGTCC | ||
NM_001029883.3:c.3575_3578delinsGGAC MANE Select | NP_001025054.1:p.Arg1192= |