HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47335030del , CM000673.2:g.47335030del | GRCh38 |
NC_000011.9:g.47356581del , CM000673.1:g.47356581del | GRCh37 |
NC_000011.8:g.47313157del | NCBI36 |
NG_007667.1:g.22675del , LRG_386:g.22675del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000545968.6:c.2905+14del MANE Select | ENSP00000442795.1:n.2905+14del | |
ENST00000256993.8:c.2905+14del | ENSP00000256993.5:n.2905+14del | |
ENST00000399249.6:c.2905+14del | ENSP00000382193.2:n.2905+14del | |
ENST00000545968.5:c.2905+14del | ENSP00000442795.1:n.2905+14del | |
NM_000256.3:c.2905+14del , LRG_386t1:c.2905+14del MANE Select | NP_000247.2:n.2905+14del | |
XM_011520117.1:c.2887+14del | XP_011518419.1:n.2887+14del | |
XM_011520118.1:c.2824+14del | XP_011518420.1:n.2824+14del |