HGVS | Genome Assembly |
---|---|
NC_000011.10:g.64753527_64753529del , CM000673.2:g.64753527_64753529del | GRCh38 |
NC_000011.9:g.64520999_64521001del , CM000673.1:g.64520999_64521001del | GRCh37 |
NC_000011.8:g.64277575_64277577del | NCBI36 |
NG_013018.1:g.12191_12193del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000164139.4:c.1397_1399del MANE Select | ENSP00000164139.3:p.Lys466del | |
ENST00000164139.3:c.1397_1399del | ENSP00000164139.3:p.Lys466del | |
ENST00000377432.7:c.1133_1135del | ENSP00000366650.3:p.Lys378del | |
NM_001164716.1:c.1133_1135del | NP_001158188.1:p.Lys378del | |
NM_005609.2:c.1397_1399del | NP_005600.1:p.Lys466del | |
NM_005609.3:c.1397_1399del | NP_005600.1:p.Lys466del | |
NM_005609.4:c.1397_1399del MANE Select | NP_005600.1:p.Lys466del |