HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1444279_1444288delinsGCGTCTACAC , CM000667.2:g.1444279_1444288delinsGCGTCTACAC | GRCh38 |
NC_000005.9:g.1444394_1444403delinsGCGTCTACAC , CM000667.1:g.1444394_1444403delinsGCGTCTACAC | GRCh37 |
NC_000005.8:g.1497394_1497403delinsGCGTCTACAC | NCBI36 |
NG_015885.1:g.6141_6150delinsGTGTAGACGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.-45-1046_-45-1037delinsGTGTAGACGC MANE Select | ENSP00000270349.9:n.-45-1046_-45-1037delinsGTGTAGACGC | |
ENST00000270349.11:c.-45-1046_-45-1037delinsGTGTAGACGC | ENSP00000270349.9:n.-45-1046_-45-1037delinsGTGTAGACGC | |
NM_001044.4:c.-45-1046_-45-1037delinsGTGTAGACGC | NP_001035.1:n.-45-1046_-45-1037delinsGTGTAGACGC | |
NM_001044.5:c.-45-1046_-45-1037delinsGTGTAGACGC MANE Select | NP_001035.1:n.-45-1046_-45-1037delinsGTGTAGACGC |