HGVS | Genome Assembly |
---|---|
NC_000011.10:g.128891465_128891476del , CM000673.2:g.128891465_128891476del | GRCh38 |
NC_000011.9:g.128761360_128761371del , CM000673.1:g.128761360_128761371del | GRCh37 |
NC_000011.8:g.128266570_128266581del | NCBI36 |
NG_023406.2:g.5048_5059del , LRG_333:g.5048_5059del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000529694.6:c.-267_-256del MANE Select | ENSP00000433295.1:n.-267_-256del | |
ENST00000529694.5:c.-267_-256del | ENSP00000433295.1:n.-267_-256del | |
NM_000890.3:c.-267_-256del , LRG_333t1:c.-267_-256del | NP_000881.3:n.-267_-256del | |
NM_000890.4:c.-267_-256del | NP_000881.3:n.-267_-256del | |
NM_001354169.1:c.-356_-345del | NP_001341098.1:n.-356_-345del | |
NM_000890.5:c.-267_-256del MANE Select | NP_000881.3:n.-267_-256del | |
NM_001354169.2:c.-356_-345del | NP_001341098.1:n.-356_-345del |