HGVS | Genome Assembly |
---|---|
NC_000011.10:g.128891435_128891456del , CM000673.2:g.128891435_128891456del | GRCh38 |
NC_000011.9:g.128761330_128761351del , CM000673.1:g.128761330_128761351del | GRCh37 |
NC_000011.8:g.128266540_128266561del | NCBI36 |
NG_023406.2:g.5018_5039del , LRG_333:g.5018_5039del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000529694.6:c.-297_-276del MANE Select | ENSP00000433295.1:n.-297_-276del | |
ENST00000529694.5:c.-297_-276del | ENSP00000433295.1:n.-297_-276del | |
NM_000890.3:c.-297_-276del , LRG_333t1:c.-297_-276del | NP_000881.3:n.-297_-276del | |
NM_000890.4:c.-297_-276del | NP_000881.3:n.-297_-276del | |
NM_001354169.1:c.-386_-365del | NP_001341098.1:n.-386_-365del | |
NM_000890.5:c.-297_-276del MANE Select | NP_000881.3:n.-297_-276del | |
NM_001354169.2:c.-386_-365del | NP_001341098.1:n.-386_-365del |