HGVS | Genome Assembly |
---|---|
NC_000012.12:g.110910990_110910994del , CM000674.2:g.110910990_110910994del | GRCh38 |
NC_000012.11:g.111348794_111348798del , CM000674.1:g.111348794_111348798del | GRCh37 |
NC_000012.10:g.109833177_109833181del | NCBI36 |
NG_007554.1:g.14584_14588del , LRG_393:g.14584_14588del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000228841.15:c.*83_*87del MANE Select | ENSP00000228841.8:n.*83_*87del | |
ENST00000663220.1:c.*83_*87del | ENSP00000499568.1:n.*83_*87del | |
ENST00000228841.12:c.*83_*87del | ENSP00000228841.7:n.*83_*87del | |
ENST00000548438.1:c.*83_*87del | ENSP00000447154.1:n.*83_*87del | |
NM_000432.3:c.*83_*87del , LRG_393t1:c.*83_*87del | NP_000423.2:n.*83_*87del | |
NM_000432.4:c.*83_*87del MANE Select | NP_000423.2:n.*83_*87del |