HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322910_73322920del , CM000677.2:g.73322910_73322920del | GRCh38 |
NC_000015.9:g.73615251_73615261del , CM000677.1:g.73615251_73615261del | GRCh37 |
NC_000015.8:g.71402304_71402314del | NCBI36 |
NG_009063.1:g.51348_51358del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.3176_3186del MANE Select | ENSP00000261917.3:p.Ser1059ThrfsTer? | |
ENST00000261917.3:c.3176_3186del | ENSP00000261917.3:p.Ser1059ThrfsTer? | |
NM_005477.2:c.3176_3186del | NP_005468.1:p.Ser1059ThrfsTer? | |
XM_011521148.1:c.1958_1968del | XP_011519450.1:p.Ser653ThrfsTer? | |
XM_011521148.2:c.1958_1968del | XP_011519450.1:p.Ser653ThrfsTer? | |
NM_005477.3:c.3176_3186del MANE Select | NP_005468.1:p.Ser1059ThrfsTer? |