Canonical Allele Identifier: CA891839432

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87957880_87957881delinsGA , CM000672.2:g.87957880_87957881delinsGA	GRCh38
NC_000010.10:g.89717637_89717638delinsGA , CM000672.1:g.89717637_89717638delinsGA	GRCh37
NC_000010.9:g.89707617_89707618delinsGA	NCBI36
NG_007466.2:g.99442_99443delinsGA , LRG_311:g.99442_99443delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.662_663delinsGA	ENSP00000514759.2:p.Lys221Arg
ENST00000710265.1:c.662_663delinsGA	ENSP00000518161.1:p.Lys221Arg
ENST00000472832.3:c.662_663delinsGA	ENSP00000483066.2:p.Lys221Arg
ENST00000688158.2:n.1397_1398delinsGA
ENST00000688922.2:c.*492_*493delinsGA	ENSP00000508742.2:n.*492_*493delinsGA
ENST00000700021.1:c.617_618delinsGA	ENSP00000514757.1:p.Lys206Arg
ENST00000700022.1:c.*1_*2delinsGA	ENSP00000514758.1:n.*1_*2delinsGA
ENST00000700023.1:n.1820_1821delinsGA
ENST00000700024.1:n.2054_2055delinsGA
ENST00000700025.1:n.1431_1432delinsGA
ENST00000700026.1:n.299_300delinsGA
ENST00000700029.1:c.496_497delinsGA
ENST00000706954.1:c.662_663delinsGA	ENSP00000516674.1:p.Lys221Arg
ENST00000706955.1:c.*697_*698delinsGA	ENSP00000516675.1:n.*697_*698delinsGA
ENST00000686459.1:c.*248_*249delinsGA	ENSP00000508909.1:n.*248_*249delinsGA
ENST00000688158.1:c.*773_*774delinsGA	ENSP00000509254.1:n.*773_*774delinsGA
ENST00000688308.1:c.662_663delinsGA	ENSP00000508752.1:p.Lys221Arg
ENST00000688922.1:c.583_584delinsGA
ENST00000693560.1:c.1181_1182delinsGA	ENSP00000509861.1:p.Lys394Arg
ENST00000371953.8:c.662_663delinsGA MANE Select	ENSP00000361021.3:p.Lys221Arg
ENST00000371953.7:c.662_663delinsGA	ENSP00000361021.3:p.Lys221Arg
ENST00000472832.2:c.89_90delinsGA	ENSP00000483066.1:p.Lys30Arg
NM_000314.5:c.662_663delinsGA	NP_000305.3:p.Lys221Arg
NM_000314.6:c.662_663delinsGA	NP_000305.3:p.Lys221Arg
NM_001304717.2:c.1181_1182delinsGA	NP_001291646.2:p.Lys394Arg
NM_001304718.1:c.71_72delinsGA	NP_001291647.1:p.Lys24Arg
XM_006717926.2:c.617_618delinsGA	XP_006717989.1:p.Lys206Arg
XM_011539981.1:c.662_663delinsGA	XP_011538283.1:p.Lys221Arg
XM_011539982.1:c.566_567delinsGA	XP_011538284.1:p.Lys189Arg
XR_945791.1:n.1232_1233delinsGA
NM_000314.7:c.662_663delinsGA	NP_000305.3:p.Lys221Arg
NM_001304717.5:c.1181_1182delinsGA	NP_001291646.4:p.Lys394Arg
NM_001304718.2:c.71_72delinsGA	NP_001291647.1:p.Lys24Arg
NM_000314.8:c.662_663delinsGA MANE Select	NP_000305.3:p.Lys221Arg