HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94989068_94989069delinsCA , CM000672.2:g.94989068_94989069delinsCA | GRCh38 |
NC_000010.10:g.96748825_96748826delinsCA , CM000672.1:g.96748825_96748826delinsCA | GRCh37 |
NC_000010.9:g.96738815_96738816delinsCA | NCBI36 |
NG_008385.1:g.55411_55412delinsCA | |
NG_008385.2:g.55911_55912delinsCA |
HGVS | Amino-acid change | |
---|---|---|
ENST00000260682.8:c.*40_*41delinsCA MANE Select | ENSP00000260682.6:n.*40_*41delinsCA | |
ENST00000643112.1:c.*522_*523delinsCA | ENSP00000496202.1:n.*522_*523delinsCA | |
ENST00000260682.6:c.*40_*41delinsCA | ENSP00000260682.6:n.*40_*41delinsCA | |
NM_000771.3:c.*40_*41delinsCA | NP_000762.2:n.*40_*41delinsCA | |
NM_000771.4:c.*40_*41delinsCA MANE Select | NP_000762.2:n.*40_*41delinsCA |