HGVS | Genome Assembly |
---|---|
NC_000010.11:g.87863039_87863040del , CM000672.2:g.87863039_87863040del | GRCh38 |
NC_000010.10:g.89622796_89622797del , CM000672.1:g.89622796_89622797del | GRCh37 |
NC_000010.9:g.89612776_89612777del | NCBI36 |
NG_007466.2:g.4602_4603del , LRG_311:g.4602_4603del | |
NG_033079.1:g.5400_5401del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706954.1:c.-17+397_-17+398del (PTEN) | ENSP00000516674.1:n.-17+397_-17+398del | |
ENST00000688308.1:c.-91_-90del (PTEN) | ENSP00000508752.1:n.-91_-90del | |
ENST00000445946.5:c.-551_-550del (KLLN) MANE Select | ENSP00000392204.2:n.-551_-550del | |
ENST00000445946.3:c.-551_-550del (KLLN) | ENSP00000392204.2:n.-551_-550del | |
NM_001126049.1:c.-551_-550del (KLLN) | NP_001119521.1:n.-551_-550del | |
NM_001126049.2:c.-551_-550del (KLLN) MANE Select | NP_001119521.1:n.-551_-550del |