HGVS | Genome Assembly |
---|---|
NC_000017.11:g.4734185_4734186insCA , CM000679.2:g.4734185_4734186insCA | GRCh38 |
NC_000017.10:g.4637480_4637481insCA , CM000679.1:g.4637480_4637481insCA | GRCh37 |
NC_000017.9:g.4584229_4584230insCA | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000293778.12:c.*317_*318insTG MANE Select | ENSP00000293778.7:n.*317_*318insTG | |
ENST00000293778.10:c.*317_*318insTG | ENSP00000293778.6:n.*317_*318insTG | |
ENST00000576153.5:n.873_874insTG | ||
NM_022059.3:c.*317_*318insTG | NP_071342.2:n.*317_*318insTG | |
NM_022059.4:c.*317_*318insTG | NP_071342.2:n.*317_*318insTG | |
NM_001386809.1:c.*317_*318insTG MANE Select | NP_001373738.1:n.*317_*318insTG |