HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87709326del , CM000672.2:g.87709326del | GRCh38 |
NC_000010.10:g.89469083del , CM000672.1:g.89469083del | GRCh37 |
NC_000010.9:g.89459063del | NCBI36 |
NG_012150.1:g.54608del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000456849.2:c.145+13del MANE Select | ENSP00000406157.1:n.145+13del | |
ENST00000361175.8:c.145+13del | ENSP00000354436.4:n.145+13del | |
ENST00000456849.1:c.145+13del | ENSP00000406157.1:n.145+13del | |
ENST00000465996.5:n.167+13del | ||
ENST00000482258.1:n.188+13del | ||
NM_001015880.1:c.145+13del | NP_001015880.1:n.145+13del | |
NM_004670.3:c.145+13del | NP_004661.2:n.145+13del | |
NM_001015880.2:c.145+13del MANE Select | NP_001015880.1:n.145+13del | |
NM_004670.4:c.145+13del | NP_004661.2:n.145+13del |