Allele Registry

HGVS	Genome Assembly
NC_000010.11:g.87863184_87863187delinsCCCG , CM000672.2:g.87863184_87863187delinsCCCG	GRCh38
NC_000010.10:g.89622941_89622944delinsCCCG , CM000672.1:g.89622941_89622944delinsCCCG	GRCh37
NC_000010.9:g.89612921_89612924delinsCCCG	NCBI36
NG_007466.2:g.4747_4750delinsCCCG , LRG_311:g.4747_4750delinsCCCG
NG_033079.1:g.5251_5254delinsCGGG

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+542_-17+545delinsCCCG (PTEN)	ENSP00000516674.1:n.-17+542_-17+545delinsCCCG
ENST00000688308.1:c.-17+71_-17+74delinsCCCG (PTEN)	ENSP00000508752.1:n.-17+71_-17+74delinsCCCG
ENST00000445946.5:c.-700_-697delinsCGGG (KLLN) MANE Select	ENSP00000392204.2:n.-700_-697delinsCGGG
ENST00000371953.7:c.-1286_-1283delinsCCCG (PTEN)	ENSP00000361021.3:n.-1286_-1283delinsCCCG
ENST00000445946.3:c.-700_-697delinsCGGG (KLLN)	ENSP00000392204.2:n.-700_-697delinsCGGG
NM_001126049.1:c.-700_-697delinsCGGG (KLLN)	NP_001119521.1:n.-700_-697delinsCGGG
NM_001126049.2:c.-700_-697delinsCGGG (KLLN) MANE Select	NP_001119521.1:n.-700_-697delinsCGGG