HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863028G= , CM000672.2:g.87863028G= | GRCh38 |
NC_000010.10:g.89622785G= , CM000672.1:g.89622785G= | GRCh37 |
NC_000010.9:g.89612765G= | NCBI36 |
NG_007466.2:g.4591G= , LRG_311:g.4591G= | |
NG_033079.1:g.5410C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+386G= (PTEN) | ENSP00000516674.1:n.-17+386G= | |
ENST00000688308.1:c.-102G= (PTEN) | ENSP00000508752.1:n.-102G= | |
ENST00000445946.5:c.-541C= (KLLN) MANE Select | ENSP00000392204.2:n.-541C= | |
ENST00000445946.3:c.-541C= (KLLN) | ENSP00000392204.2:n.-541C= | |
NM_001126049.1:c.-541C= (KLLN) | NP_001119521.1:n.-541C= | |
NM_001126049.2:c.-541C= (KLLN) MANE Select | NP_001119521.1:n.-541C= |