HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29071047_29071048insA , CM000664.2:g.29071047_29071048insA | GRCh38 |
NC_000002.11:g.29293913_29293914insA , CM000664.1:g.29293913_29293914insA | GRCh37 |
NC_000002.10:g.29147417_29147418insA | NCBI36 |
NG_021427.1:g.8214_8215insT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.3214_3215insT MANE Select | ENSP00000332809.4:p.Ser1072MetfsTer? | |
ENST00000331664.5:c.3214_3215insT | ENSP00000332809.4:p.Ser1072MetfsTer? | |
NM_001029883.2:c.3214_3215insT | NP_001025054.1:p.Ser1072MetfsTer? | |
XM_011532826.1:c.3214_3215insT | XP_011531128.1:p.Ser1072MetfsTer? | |
XR_939901.1:n.185+1880_185+1881insA | ||
XR_939902.1:n.173+1892_173+1893insA | ||
NM_001029883.3:c.3214_3215insT MANE Select | NP_001025054.1:p.Ser1072MetfsTer? |