Allele Registry

HGVS	Genome Assembly
NC_000010.11:g.87863155_87863157delinsATC , CM000672.2:g.87863155_87863157delinsATC	GRCh38
NC_000010.10:g.89622912_89622914delinsATC , CM000672.1:g.89622912_89622914delinsATC	GRCh37
NC_000010.9:g.89612892_89612894delinsATC	NCBI36
NG_007466.2:g.4718_4720delinsATC , LRG_311:g.4718_4720delinsATC
NG_033079.1:g.5281_5283delinsGAT

HGVS	Amino-acid Change
ENST00000706954.1:c.-17+513_-17+515delinsATC (PTEN)	ENSP00000516674.1:n.-17+513_-17+515delinsATC
ENST00000688308.1:c.-17+42_-17+44delinsATC (PTEN)	ENSP00000508752.1:n.-17+42_-17+44delinsATC
ENST00000445946.5:c.-670_-668delinsGAT (KLLN) MANE Select	ENSP00000392204.2:n.-670_-668delinsGAT
ENST00000371953.7:c.-1315_-1313delinsATC (PTEN)	ENSP00000361021.3:n.-1315_-1313delinsATC
ENST00000445946.3:c.-670_-668delinsGAT (KLLN)	ENSP00000392204.2:n.-670_-668delinsGAT
NM_001126049.1:c.-670_-668delinsGAT (KLLN)	NP_001119521.1:n.-670_-668delinsGAT
NM_001126049.2:c.-670_-668delinsGAT (KLLN) MANE Select	NP_001119521.1:n.-670_-668delinsGAT