HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863349T= , CM000672.2:g.87863349T= | GRCh38 |
NC_000010.10:g.89623106T= , CM000672.1:g.89623106T= | GRCh37 |
NC_000010.9:g.89613086T= | NCBI36 |
NG_007466.2:g.4912T= , LRG_311:g.4912T= | |
NG_033079.1:g.5089A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+707T= (PTEN) | ENSP00000516674.1:n.-17+707T= | |
ENST00000688308.1:c.-17+236T= (PTEN) | ENSP00000508752.1:n.-17+236T= | |
ENST00000445946.5:c.-862A= (KLLN) MANE Select | ENSP00000392204.2:n.-862A= | |
ENST00000371953.7:c.-1121T= (PTEN) | ENSP00000361021.3:n.-1121T= | |
ENST00000445946.3:c.-862A= (KLLN) | ENSP00000392204.2:n.-862A= | |
NM_001126049.1:c.-862A= (KLLN) | NP_001119521.1:n.-862A= | |
NM_001126049.2:c.-862A= (KLLN) MANE Select | NP_001119521.1:n.-862A= |