HGVS | Genome Assembly |
---|---|
NC_000006.12:g.31269157_31269158insT , CM000668.2:g.31269157_31269158insT | GRCh38 |
NC_000006.11:g.31236934_31236935insT , CM000668.1:g.31236934_31236935insT | GRCh37 |
NC_000006.10:g.31344913_31344914insT | NCBI36 |
NG_029422.2:g.7974_7975insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000376228.10:c.*11_*12insA MANE Select | ENSP00000365402.5:n.*11_*12insA | |
ENST00000376228.9:c.*11_*12insA | ENSP00000365402.5:n.*11_*12insA | |
ENST00000376237.8:c.*699_*700insA | ENSP00000365412.4:n.*699_*700insA | |
ENST00000383329.7:c.*11_*12insA | ENSP00000372819.3:n.*11_*12insA | |
ENST00000466892.5:n.345_346insA | ||
ENST00000470363.5:n.870_871insA | ||
ENST00000487245.5:n.1471_1472insA | ||
NM_002117.5:c.*11_*12insA | NP_002108.4:n.*11_*12insA | |
NM_002117.6:c.*11_*12insA MANE Select | NP_002108.4:n.*11_*12insA |