HGVS | Genome Assembly |
---|---|
NC_000017.11:g.43755307_43755332delinsGGGCGCCCGCCGGTGGGGAGGGGCGC , CM000679.2:g.43755307_43755332delinsGGGCGCCCGCCGGTGGGGAGGGGCGC | GRCh38 |
NC_000017.10:g.41832675_41832700delinsGGGCGCCCGCCGGTGGGGAGGGGCGC , CM000679.1:g.41832675_41832700delinsGGGCGCCCGCCGGTGGGGAGGGGCGC | GRCh37 |
NC_000017.9:g.39188201_39188226delinsGGGCGCCCGCCGGTGGGGAGGGGCGC | NCBI36 |
NG_008078.2:g.8457_8482delinsGCGCCCCTCCCCACCGGCGGGCGCCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301691.3:c.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC MANE Select | ENSP00000301691.1:n.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC | |
ENST00000301691.2:c.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC | ENSP00000301691.1:n.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC | |
NM_025237.2:c.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC | NP_079513.1:n.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC | |
NM_025237.3:c.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC MANE Select | NP_079513.1:n.*10_*35delinsGCGCCCCTCCCCACCGGCGGGCGCCC |