HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863231A>T , CM000672.2:g.87863231A>T | GRCh38 |
NC_000010.10:g.89622988A>T , CM000672.1:g.89622988A>T | GRCh37 |
NC_000010.9:g.89612968A>T | NCBI36 |
NG_007466.2:g.4794A>T , LRG_311:g.4794A>T | |
NG_033079.1:g.5207T>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+589A>T (PTEN) | ENSP00000516674.1:n.-17+589A>T | |
ENST00000688308.1:c.-17+118A>T (PTEN) | ENSP00000508752.1:n.-17+118A>T | |
ENST00000445946.5:c.-744T>A (KLLN) MANE Select | ENSP00000392204.2:n.-744T>A | |
ENST00000371953.7:c.-1239A>T (PTEN) | ENSP00000361021.3:n.-1239A>T | |
ENST00000445946.3:c.-744T>A (KLLN) | ENSP00000392204.2:n.-744T>A | |
NM_001126049.1:c.-744T>A (KLLN) | NP_001119521.1:n.-744T>A | |
NM_001126049.2:c.-744T>A (KLLN) MANE Select | NP_001119521.1:n.-744T>A |