HGVS | Genome Assembly |
---|---|
NC_000019.10:g.2251407_2251493del , CM000681.2:g.2251407_2251493del | GRCh38 |
NC_000019.9:g.2251406_2251492del , CM000681.1:g.2251406_2251492del | GRCh37 |
NC_000019.8:g.2202406_2202492del | NCBI36 |
NG_012190.1:g.7294_7380del | |
NG_032853.1:g.9941_10027del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000221496.5:c.1133_1219del MANE Select | ENSP00000221496.2:p.Arg378_Arg406del | |
ENST00000221496.4:c.1133_1219del | ENSP00000221496.2:p.Arg378_Arg406del | |
ENST00000589313.2:n.1486_1572del | ||
NM_000479.3:c.1133_1219del | NP_000470.2:p.Arg378_Arg406del | |
NM_000479.4:c.1133_1219del | NP_000470.2:p.Arg378_Arg406del | |
NM_000479.5:c.1133_1219del MANE Select | NP_000470.3:p.Arg378_Arg406del |