HGVS | Genome Assembly |
---|---|
NC_000019.10:g.55151776del , CM000681.2:g.55151776del | GRCh38 |
NC_000019.9:g.55663144del , CM000681.1:g.55663144del | GRCh37 |
NC_000019.8:g.60354956del | NCBI36 |
NG_007866.2:g.10957del , LRG_432:g.10957del | |
NG_011829.2:g.2463del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000344887.10:c.*58del MANE Select | ENSP00000341838.5:n.*58del | |
ENST00000665070.1:c.*58del | ENSP00000499482.1:n.*58del | |
ENST00000344887.9:c.*58del | ENSP00000341838.5:n.*58del | |
ENST00000585806.5:n.690del | ||
ENST00000588882.1:c.*58del | ENSP00000466729.1:n.*58del | |
ENST00000589864.1:n.519del | ||
NM_000363.4:c.*58del , LRG_432t1:c.*58del | NP_000354.4:n.*58del | |
NM_000363.5:c.*58del MANE Select | NP_000354.4:n.*58del |