HGVS | Genome Assembly |
---|---|
NC_000008.11:g.109087644_109087646del , CM000670.2:g.109087644_109087646del | GRCh38 |
NC_000008.10:g.110099873_110099875del , CM000670.1:g.110099873_110099875del | GRCh37 |
NC_000008.9:g.110169049_110169051del | NCBI36 |
NG_017161.1:g.5198_5200del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000518632.2:c.132_134del MANE Select | ENSP00000430711.2:p.Ile44del | |
ENST00000311762.2:c.132_134del | ENSP00000309818.2:p.Ile44del | |
ENST00000518632.1:c.132_134del | ENSP00000430711.1:p.Ile44del | |
NM_003301.5:c.132_134del | NP_003292.1:p.Ile44del | |
XM_011517263.1:c.132_134del | XP_011515565.1:p.Ile44del | |
XM_011517263.2:c.132_134del | XP_011515565.1:p.Ile44del | |
NM_003301.7:c.132_134del MANE Select | NP_003292.1:p.Ile44del |