Canonical Allele Identifier: CA891835062

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925541_87925543delinsGTT , CM000672.2:g.87925541_87925543delinsGTT	GRCh38
NC_000010.10:g.89685298_89685300delinsGTT , CM000672.1:g.89685298_89685300delinsGTT	GRCh37
NC_000010.9:g.89675278_89675280delinsGTT	NCBI36
NG_007466.2:g.67103_67105delinsGTT , LRG_311:g.67103_67105delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.193_195delinsGTT	ENSP00000514759.2:p.Tyr65Val
ENST00000710265.1:c.193_195delinsGTT	ENSP00000518161.1:p.Tyr65Val
ENST00000472832.3:c.193_195delinsGTT	ENSP00000483066.2:p.Tyr65Val
ENST00000688158.2:n.928_930delinsGTT
ENST00000688922.2:c.193_195delinsGTT	ENSP00000508742.2:p.Tyr65Val
ENST00000700021.1:c.165-5505_165-5503delinsGTT	ENSP00000514757.1:n.165-5505_165-5503delinsGTT
ENST00000700022.1:c.193_195delinsGTT	ENSP00000514758.1:p.Tyr65Val
ENST00000700029.1:c.27_29delinsGTT
ENST00000706954.1:c.193_195delinsGTT	ENSP00000516674.1:p.Tyr65Val
ENST00000706955.1:c.*228_*230delinsGTT	ENSP00000516675.1:n.*228_*230delinsGTT
ENST00000686459.1:c.193_195delinsGTT	ENSP00000508909.1:p.Tyr65Val
ENST00000688158.1:c.*304_*306delinsGTT	ENSP00000509254.1:n.*304_*306delinsGTT
ENST00000688308.1:c.193_195delinsGTT	ENSP00000508752.1:p.Tyr65Val
ENST00000688922.1:c.62_64delinsGTT
ENST00000693560.1:c.712_714delinsGTT	ENSP00000509861.1:p.Tyr238Val
ENST00000371953.8:c.193_195delinsGTT MANE Select	ENSP00000361021.3:p.Tyr65Val
ENST00000371953.7:c.193_195delinsGTT	ENSP00000361021.3:p.Tyr65Val
ENST00000498703.1:n.19_21delinsGTT
ENST00000610634.1:c.91_93delinsGTT	ENSP00000477517.1:p.Tyr31Val
NM_000314.5:c.193_195delinsGTT	NP_000305.3:p.Tyr65Val
NM_000314.6:c.193_195delinsGTT	NP_000305.3:p.Tyr65Val
NM_001304717.2:c.712_714delinsGTT	NP_001291646.2:p.Tyr238Val
NM_001304718.1:c.-541-5505_-541-5503delinsGTT	NP_001291647.1:n.-541-5505_-541-5503delinsGTT
XM_006717926.2:c.165-5505_165-5503delinsGTT	XP_006717989.1:n.165-5505_165-5503delinsGTT
XM_011539981.1:c.193_195delinsGTT	XP_011538283.1:p.Tyr65Val
XM_011539982.1:c.97_99delinsGTT	XP_011538284.1:p.Tyr33Val
XR_945789.1:n.905_907delinsGTT
XR_945790.1:n.905_907delinsGTT
XR_945791.1:n.905_907delinsGTT
NM_000314.7:c.193_195delinsGTT	NP_000305.3:p.Tyr65Val
NM_001304717.5:c.712_714delinsGTT	NP_001291646.4:p.Tyr238Val
NM_001304718.2:c.-541-5505_-541-5503delinsGTT	NP_001291647.1:n.-541-5505_-541-5503delinsGTT
NM_000314.8:c.193_195delinsGTT MANE Select	NP_000305.3:p.Tyr65Val