HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1444262_1444270delinsTGAGCAGGA , CM000667.2:g.1444262_1444270delinsTGAGCAGGA | GRCh38 |
NC_000005.9:g.1444377_1444385delinsTGAGCAGGA , CM000667.1:g.1444377_1444385delinsTGAGCAGGA | GRCh37 |
NC_000005.8:g.1497377_1497385delinsTGAGCAGGA | NCBI36 |
NG_015885.1:g.6159_6167delinsTCCTGCTCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270349.12:c.-45-1028_-45-1020delinsTCCTGCTCA MANE Select | ENSP00000270349.9:n.-45-1028_-45-1020delinsTCCTGCTCA | |
ENST00000270349.11:c.-45-1028_-45-1020delinsTCCTGCTCA | ENSP00000270349.9:n.-45-1028_-45-1020delinsTCCTGCTCA | |
NM_001044.4:c.-45-1028_-45-1020delinsTCCTGCTCA | NP_001035.1:n.-45-1028_-45-1020delinsTCCTGCTCA | |
NM_001044.5:c.-45-1028_-45-1020delinsTCCTGCTCA MANE Select | NP_001035.1:n.-45-1028_-45-1020delinsTCCTGCTCA |