Canonical Allele Identifier: CA2579926611

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961098_87961100delinsACT , CM000672.2:g.87961098_87961100delinsACT	GRCh38
NC_000010.10:g.89720855_89720857delinsACT , CM000672.1:g.89720855_89720857delinsACT	GRCh37
NC_000010.9:g.89710835_89710837delinsACT	NCBI36
NG_007466.2:g.102660_102662delinsACT , LRG_311:g.102660_102662delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1099_1101delinsACT	ENSP00000514759.2:p.Tyr367Thr
ENST00000710265.1:c.1006_1008delinsACT	ENSP00000518161.1:p.Tyr336Thr
ENST00000472832.3:c.1006_1008delinsACT	ENSP00000483066.2:p.Tyr336Thr
ENST00000688158.2:n.1741_1743delinsACT
ENST00000688922.2:c.*836_*838delinsACT	ENSP00000508742.2:n.*836_*838delinsACT
ENST00000700021.1:c.961_963delinsACT	ENSP00000514757.1:p.Tyr321Thr
ENST00000700022.1:c.*345_*347delinsACT	ENSP00000514758.1:n.*345_*347delinsACT
ENST00000700023.1:n.2164_2166delinsACT
ENST00000700024.1:n.2398_2400delinsACT
ENST00000700025.1:n.1775_1777delinsACT
ENST00000700026.1:n.643_645delinsACT
ENST00000706954.1:c.1006_1008delinsACT	ENSP00000516674.1:p.Tyr336Thr
ENST00000706955.1:c.*1041_*1043delinsACT	ENSP00000516675.1:n.*1041_*1043delinsACT
ENST00000686459.1:c.*592_*594delinsACT	ENSP00000508909.1:n.*592_*594delinsACT
ENST00000688158.1:c.*1117_*1119delinsACT	ENSP00000509254.1:n.*1117_*1119delinsACT
ENST00000688308.1:c.1006_1008delinsACT	ENSP00000508752.1:p.Tyr336Thr
ENST00000688922.1:c.927_929delinsACT
ENST00000693560.1:c.1525_1527delinsACT	ENSP00000509861.1:p.Tyr509Thr
ENST00000371953.8:c.1006_1008delinsACT MANE Select	ENSP00000361021.3:p.Tyr336Thr
ENST00000371953.7:c.1006_1008delinsACT	ENSP00000361021.3:p.Tyr336Thr
ENST00000472832.2:c.433_435delinsACT	ENSP00000483066.1:p.Tyr145Thr
NM_000314.5:c.1006_1008delinsACT	NP_000305.3:p.Tyr336Thr
NM_000314.6:c.1006_1008delinsACT	NP_000305.3:p.Tyr336Thr
NM_001304717.2:c.1525_1527delinsACT	NP_001291646.2:p.Tyr509Thr
NM_001304718.1:c.415_417delinsACT	NP_001291647.1:p.Tyr139Thr
XM_006717926.2:c.961_963delinsACT	XP_006717989.1:p.Tyr321Thr
XM_011539981.1:c.1006_1008delinsACT	XP_011538283.1:p.Tyr336Thr
XM_011539982.1:c.910_912delinsACT	XP_011538284.1:p.Tyr304Thr
XR_945791.1:n.1576_1578delinsACT
NM_000314.7:c.1006_1008delinsACT	NP_000305.3:p.Tyr336Thr
NM_001304717.5:c.1525_1527delinsACT	NP_001291646.4:p.Tyr509Thr
NM_001304718.2:c.415_417delinsACT	NP_001291647.1:p.Tyr139Thr
NM_000314.8:c.1006_1008delinsACT MANE Select	NP_000305.3:p.Tyr336Thr