HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863359A>T , CM000672.2:g.87863359A>T | GRCh38 |
NC_000010.10:g.89623116A>T , CM000672.1:g.89623116A>T | GRCh37 |
NC_000010.9:g.89613096A>T | NCBI36 |
NG_007466.2:g.4922A>T , LRG_311:g.4922A>T | |
NG_033079.1:g.5079T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+717A>T (PTEN) | ENSP00000516674.1:n.-17+717A>T | |
ENST00000688308.1:c.-17+246A>T (PTEN) | ENSP00000508752.1:n.-17+246A>T | |
ENST00000445946.5:c.-872T>A (KLLN) MANE Select | ENSP00000392204.2:n.-872T>A | |
ENST00000371953.7:c.-1111A>T (PTEN) | ENSP00000361021.3:n.-1111A>T | |
ENST00000445946.3:c.-872T>A (KLLN) | ENSP00000392204.2:n.-872T>A | |
NM_001126049.1:c.-872T>A (KLLN) | NP_001119521.1:n.-872T>A | |
NM_001126049.2:c.-872T>A (KLLN) MANE Select | NP_001119521.1:n.-872T>A |