HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73329766del , CM000677.2:g.73329766del | GRCh38 |
NC_000015.9:g.73622107del , CM000677.1:g.73622107del | GRCh37 |
NC_000015.8:g.71409160del | NCBI36 |
NG_009063.1:g.44500del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.1398del MANE Select | ENSP00000261917.3:p.Tyr467ThrfsTer7 | |
ENST00000261917.3:c.1398del | ENSP00000261917.3:p.Tyr467ThrfsTer7 | |
NM_005477.2:c.1398del | NP_005468.1:p.Tyr467ThrfsTer7 | |
XM_011521148.1:c.180del | XP_011519450.1:p.Tyr61ThrfsTer7 | |
XM_011521148.2:c.180del | XP_011519450.1:p.Tyr61ThrfsTer7 | |
NM_005477.3:c.1398del MANE Select | NP_005468.1:p.Tyr467ThrfsTer7 |