HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47334916del , CM000673.2:g.47334916del | GRCh38 |
NC_000011.9:g.47356467del , CM000673.1:g.47356467del | GRCh37 |
NC_000011.8:g.47313043del | NCBI36 |
NG_007667.1:g.22790del , LRG_386:g.22790del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000545968.6:c.2905+129del MANE Select | ENSP00000442795.1:n.2905+129del | |
ENST00000256993.8:c.2905+129del | ENSP00000256993.5:n.2905+129del | |
ENST00000399249.6:c.2905+129del | ENSP00000382193.2:n.2905+129del | |
ENST00000545968.5:c.2905+129del | ENSP00000442795.1:n.2905+129del | |
NM_000256.3:c.2905+129del , LRG_386t1:c.2905+129del MANE Select | NP_000247.2:n.2905+129del | |
XM_011520117.1:c.2887+129del | XP_011518419.1:n.2887+129del | |
XM_011520118.1:c.2824+129del | XP_011518420.1:n.2824+129del |