HGVS | Genome Assembly |
---|---|
NC_000013.11:g.48303990_48303992del , CM000675.2:g.48303990_48303992del | GRCh38 |
NC_000013.10:g.48878126_48878128del , CM000675.1:g.48878126_48878128del | GRCh37 |
NC_000013.9:g.47776127_47776129del | NCBI36 |
NG_009009.1:g.5244_5246del , LRG_517:g.5244_5246del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000267163.6:c.78_80del MANE Select | ENSP00000267163.4:p.Pro27del | |
ENST00000646097.1:c.78_80del | ENSP00000496556.1:p.Pro27del | |
ENST00000650461.1:c.78_80del | ENSP00000497193.1:p.Pro27del | |
ENST00000267163.4:c.78_80del | ENSP00000267163.4:p.Pro27del | |
ENST00000467505.5:c.78_80del | ENSP00000434702.1:p.Pro27del | |
ENST00000525036.1:n.240_242del | ||
NM_000321.2:c.78_80del , LRG_517t1:c.78_80del | NP_000312.2:p.Pro27del | |
NM_000321.3:c.78_80del MANE Select | NP_000312.2:p.Pro27del |