Allele Registry

HGVS	Genome Assembly
NC_000010.11:g.87863287_87863304delinsTGCAGCTGCAGGCTGGCG , CM000672.2:g.87863287_87863304delinsTGCAGCTGCAGGCTGGCG	GRCh38
NC_000010.10:g.89623044_89623061delinsTGCAGCTGCAGGCTGGCG , CM000672.1:g.89623044_89623061delinsTGCAGCTGCAGGCTGGCG	GRCh37
NC_000010.9:g.89613024_89613041delinsTGCAGCTGCAGGCTGGCG	NCBI36
NG_007466.2:g.4850_4867delinsTGCAGCTGCAGGCTGGCG , LRG_311:g.4850_4867delinsTGCAGCTGCAGGCTGGCG
NG_033079.1:g.5134_5151delinsCGCCAGCCTGCAGCTGCA

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+645_-17+662delinsTGCAGCTGCAGGCTGGCG (PTEN)	ENSP00000516674.1:n.-17+645_-17+662delinsTGCAGCTGCAGGCTGGCG
ENST00000688308.1:c.-17+174_-17+191delinsTGCAGCTGCAGGCTGGCG (PTEN)	ENSP00000508752.1:n.-17+174_-17+191delinsTGCAGCTGCAGGCTGGCG
ENST00000445946.5:c.-817_-800delinsCGCCAGCCTGCAGCTGCA (KLLN) MANE Select	ENSP00000392204.2:n.-817_-800delinsCGCCAGCCTGCAGCTGCA
ENST00000371953.7:c.-1183_-1166delinsTGCAGCTGCAGGCTGGCG (PTEN)	ENSP00000361021.3:n.-1183_-1166delinsTGCAGCTGCAGGCTGGCG
ENST00000445946.3:c.-817_-800delinsCGCCAGCCTGCAGCTGCA (KLLN)	ENSP00000392204.2:n.-817_-800delinsCGCCAGCCTGCAGCTGCA
NM_001126049.1:c.-817_-800delinsCGCCAGCCTGCAGCTGCA (KLLN)	NP_001119521.1:n.-817_-800delinsCGCCAGCCTGCAGCTGCA
NM_001126049.2:c.-817_-800delinsCGCCAGCCTGCAGCTGCA (KLLN) MANE Select	NP_001119521.1:n.-817_-800delinsCGCCAGCCTGCAGCTGCA