HGVS | Genome Assembly |
---|---|
NC_000011.10:g.116778230_116778234del , CM000673.2:g.116778230_116778234del | GRCh38 |
NC_000011.9:g.116648946_116648950del , CM000673.1:g.116648946_116648950del | GRCh37 |
NC_000011.8:g.116154156_116154160del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000227322.8:c.*691_*695del MANE Select | ENSP00000227322.3:n.*691_*695del | |
ENST00000227322.7:c.*691_*695del | ENSP00000227322.3:n.*691_*695del | |
ENST00000429220.5:c.1850_1854del | ||
ENST00000444935.5:c.1983_1987del | ||
NM_001317086.1:c.*691_*695del | NP_001304015.1:n.*691_*695del | |
NM_003904.4:c.*691_*695del | NP_003895.1:n.*691_*695del | |
NM_003904.5:c.*691_*695del MANE Select | NP_003895.1:n.*691_*695del | |
NM_001317086.2:c.*691_*695del | NP_001304015.1:n.*691_*695del |