HGVS | Genome Assembly |
---|---|
NC_000014.9:g.24256109_24256111del , CM000676.2:g.24256109_24256111del | GRCh38 |
NC_000014.8:g.24725315_24725317del , CM000676.1:g.24725315_24725317del | GRCh37 |
NC_000014.7:g.23795155_23795157del | NCBI36 |
NG_007150.1:g.12056_12058del | |
NG_007150.2:g.12056_12058del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000206765.11:c.1403-34_1403-32del MANE Select | ENSP00000206765.6:n.1403-34_1403-32del | |
ENST00000206765.10:c.1403-34_1403-32del | ENSP00000206765.6:n.1403-34_1403-32del | |
ENST00000544573.5:c.77-34_77-32del | ENSP00000439446.1:n.77-34_77-32del | |
ENST00000559136.1:c.476-34_476-32del | ENSP00000453337.1:n.476-34_476-32del | |
NM_000359.2:c.1403-34_1403-32del | NP_000350.1:n.1403-34_1403-32del | |
NM_000359.3:c.1403-34_1403-32del MANE Select | NP_000350.1:n.1403-34_1403-32del |