Allele Registry

HGVS	Genome Assembly
NC_000010.11:g.87863278_87863281delinsCGCA , CM000672.2:g.87863278_87863281delinsCGCA	GRCh38
NC_000010.10:g.89623035_89623038delinsCGCA , CM000672.1:g.89623035_89623038delinsCGCA	GRCh37
NC_000010.9:g.89613015_89613018delinsCGCA	NCBI36
NG_007466.2:g.4841_4844delinsCGCA , LRG_311:g.4841_4844delinsCGCA
NG_033079.1:g.5157_5160delinsTGCG

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+636_-17+639delinsCGCA (PTEN)	ENSP00000516674.1:n.-17+636_-17+639delinsCGCA
ENST00000688308.1:c.-17+165_-17+168delinsCGCA (PTEN)	ENSP00000508752.1:n.-17+165_-17+168delinsCGCA
ENST00000445946.5:c.-794_-791delinsTGCG (KLLN) MANE Select	ENSP00000392204.2:n.-794_-791delinsTGCG
ENST00000371953.7:c.-1192_-1189delinsCGCA (PTEN)	ENSP00000361021.3:n.-1192_-1189delinsCGCA
ENST00000445946.3:c.-794_-791delinsTGCG (KLLN)	ENSP00000392204.2:n.-794_-791delinsTGCG
NM_001126049.1:c.-794_-791delinsTGCG (KLLN)	NP_001119521.1:n.-794_-791delinsTGCG
NM_001126049.2:c.-794_-791delinsTGCG (KLLN) MANE Select	NP_001119521.1:n.-794_-791delinsTGCG