HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94775463del , CM000672.2:g.94775463del | GRCh38 |
NC_000010.10:g.96535220del , CM000672.1:g.96535220del | GRCh37 |
NC_000010.9:g.96525210del | NCBI36 |
NG_008384.2:g.17758del | |
NG_008384.3:g.17783del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.405del MANE Select | ENSP00000360372.3:p.Met136TrpfsTer21 | |
ENST00000645461.1:n.1458del | ||
ENST00000371321.7:c.405del | ENSP00000360372.3:p.Met136TrpfsTer21 | |
ENST00000464755.1:c.1168del | ENSP00000483243.1:n.1168del | |
ENST00000480405.2:c.405del | ENSP00000483847.1:p.Met136TrpfsTer21 | |
NM_000769.2:c.405del | NP_000760.1:p.Met136TrpfsTer21 | |
NM_000769.4:c.405del MANE Select | NP_000760.1:p.Met136TrpfsTer21 |