Canonical Allele Identifier: CA891835114

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925545_87925546delinsCT , CM000672.2:g.87925545_87925546delinsCT	GRCh38
NC_000010.10:g.89685302_89685303delinsCT , CM000672.1:g.89685302_89685303delinsCT	GRCh37
NC_000010.9:g.89675282_89675283delinsCT	NCBI36
NG_007466.2:g.67107_67108delinsCT , LRG_311:g.67107_67108delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.197_198delinsCT	ENSP00000514759.2:p.Lys66Thr
ENST00000710265.1:c.197_198delinsCT	ENSP00000518161.1:p.Lys66Thr
ENST00000472832.3:c.197_198delinsCT	ENSP00000483066.2:p.Lys66Thr
ENST00000688158.2:n.932_933delinsCT
ENST00000688922.2:c.197_198delinsCT	ENSP00000508742.2:p.Lys66Thr
ENST00000700021.1:c.165-5501_165-5500delinsCT	ENSP00000514757.1:n.165-5501_165-5500delinsCT
ENST00000700022.1:c.197_198delinsCT	ENSP00000514758.1:p.Lys66Thr
ENST00000700029.1:c.31_32delinsCT
ENST00000706954.1:c.197_198delinsCT	ENSP00000516674.1:p.Lys66Thr
ENST00000706955.1:c.*232_*233delinsCT	ENSP00000516675.1:n.*232_*233delinsCT
ENST00000686459.1:c.197_198delinsCT	ENSP00000508909.1:p.Lys66Thr
ENST00000688158.1:c.*308_*309delinsCT	ENSP00000509254.1:n.*308_*309delinsCT
ENST00000688308.1:c.197_198delinsCT	ENSP00000508752.1:p.Lys66Thr
ENST00000688922.1:c.66_67delinsCT
ENST00000693560.1:c.716_717delinsCT	ENSP00000509861.1:p.Lys239Thr
ENST00000371953.8:c.197_198delinsCT MANE Select	ENSP00000361021.3:p.Lys66Thr
ENST00000371953.7:c.197_198delinsCT	ENSP00000361021.3:p.Lys66Thr
ENST00000498703.1:n.23_24delinsCT
ENST00000610634.1:c.95_96delinsCT	ENSP00000477517.1:p.Lys32Thr
NM_000314.5:c.197_198delinsCT	NP_000305.3:p.Lys66Thr
NM_000314.6:c.197_198delinsCT	NP_000305.3:p.Lys66Thr
NM_001304717.2:c.716_717delinsCT	NP_001291646.2:p.Lys239Thr
NM_001304718.1:c.-541-5501_-541-5500delinsCT	NP_001291647.1:n.-541-5501_-541-5500delinsCT
XM_006717926.2:c.165-5501_165-5500delinsCT	XP_006717989.1:n.165-5501_165-5500delinsCT
XM_011539981.1:c.197_198delinsCT	XP_011538283.1:p.Lys66Thr
XM_011539982.1:c.101_102delinsCT	XP_011538284.1:p.Lys34Thr
XR_945789.1:n.909_910delinsCT
XR_945790.1:n.909_910delinsCT
XR_945791.1:n.909_910delinsCT
NM_000314.7:c.197_198delinsCT	NP_000305.3:p.Lys66Thr
NM_001304717.5:c.716_717delinsCT	NP_001291646.4:p.Lys239Thr
NM_001304718.2:c.-541-5501_-541-5500delinsCT	NP_001291647.1:n.-541-5501_-541-5500delinsCT
NM_000314.8:c.197_198delinsCT MANE Select	NP_000305.3:p.Lys66Thr