HGVS | Genome Assembly |
---|---|
NC_000022.11:g.19724401del , CM000684.2:g.19724401del | GRCh38 |
NC_000022.10:g.19711924del , CM000684.1:g.19711924del | GRCh37 |
NC_000022.9:g.18091924del | NCBI36 |
NG_007974.1:g.5859del , LRG_478:g.5859del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366425.4:c.558del (GP1BB) MANE Select | ENSP00000383382.2:p.Ala187GlnfsTer6 | |
ENST00000366425.3:c.558del (GP1BB) | ENSP00000383382.2:p.Ala187GlnfsTer6 | |
ENST00000431044.5:c.*1643del (SEPTIN5) | ENSP00000399685.1:n.*1643del | |
NM_000407.4:c.558del , LRG_478t1:c.558del (GP1BB) | NP_000398.1:p.Ala187GlnfsTer6 | |
NR_037611.1:n.4298del | ||
NR_037612.1:n.2802del | ||
NM_000407.5:c.558del (GP1BB) MANE Select | NP_000398.1:p.Ala187GlnfsTer6 |