Canonical Allele Identifier: CA2579926610

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961098_87961100delinsGGT , CM000672.2:g.87961098_87961100delinsGGT	GRCh38
NC_000010.10:g.89720855_89720857delinsGGT , CM000672.1:g.89720855_89720857delinsGGT	GRCh37
NC_000010.9:g.89710835_89710837delinsGGT	NCBI36
NG_007466.2:g.102660_102662delinsGGT , LRG_311:g.102660_102662delinsGGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1099_1101delinsGGT	ENSP00000514759.2:p.Tyr367Gly
ENST00000710265.1:c.1006_1008delinsGGT	ENSP00000518161.1:p.Tyr336Gly
ENST00000472832.3:c.1006_1008delinsGGT	ENSP00000483066.2:p.Tyr336Gly
ENST00000688158.2:n.1741_1743delinsGGT
ENST00000688922.2:c.*836_*838delinsGGT	ENSP00000508742.2:n.*836_*838delinsGGT
ENST00000700021.1:c.961_963delinsGGT	ENSP00000514757.1:p.Tyr321Gly
ENST00000700022.1:c.*345_*347delinsGGT	ENSP00000514758.1:n.*345_*347delinsGGT
ENST00000700023.1:n.2164_2166delinsGGT
ENST00000700024.1:n.2398_2400delinsGGT
ENST00000700025.1:n.1775_1777delinsGGT
ENST00000700026.1:n.643_645delinsGGT
ENST00000706954.1:c.1006_1008delinsGGT	ENSP00000516674.1:p.Tyr336Gly
ENST00000706955.1:c.*1041_*1043delinsGGT	ENSP00000516675.1:n.*1041_*1043delinsGGT
ENST00000686459.1:c.*592_*594delinsGGT	ENSP00000508909.1:n.*592_*594delinsGGT
ENST00000688158.1:c.*1117_*1119delinsGGT	ENSP00000509254.1:n.*1117_*1119delinsGGT
ENST00000688308.1:c.1006_1008delinsGGT	ENSP00000508752.1:p.Tyr336Gly
ENST00000688922.1:c.927_929delinsGGT
ENST00000693560.1:c.1525_1527delinsGGT	ENSP00000509861.1:p.Tyr509Gly
ENST00000371953.8:c.1006_1008delinsGGT MANE Select	ENSP00000361021.3:p.Tyr336Gly
ENST00000371953.7:c.1006_1008delinsGGT	ENSP00000361021.3:p.Tyr336Gly
ENST00000472832.2:c.433_435delinsGGT	ENSP00000483066.1:p.Tyr145Gly
NM_000314.5:c.1006_1008delinsGGT	NP_000305.3:p.Tyr336Gly
NM_000314.6:c.1006_1008delinsGGT	NP_000305.3:p.Tyr336Gly
NM_001304717.2:c.1525_1527delinsGGT	NP_001291646.2:p.Tyr509Gly
NM_001304718.1:c.415_417delinsGGT	NP_001291647.1:p.Tyr139Gly
XM_006717926.2:c.961_963delinsGGT	XP_006717989.1:p.Tyr321Gly
XM_011539981.1:c.1006_1008delinsGGT	XP_011538283.1:p.Tyr336Gly
XM_011539982.1:c.910_912delinsGGT	XP_011538284.1:p.Tyr304Gly
XR_945791.1:n.1576_1578delinsGGT
NM_000314.7:c.1006_1008delinsGGT	NP_000305.3:p.Tyr336Gly
NM_001304717.5:c.1525_1527delinsGGT	NP_001291646.4:p.Tyr509Gly
NM_001304718.2:c.415_417delinsGGT	NP_001291647.1:p.Tyr139Gly
NM_000314.8:c.1006_1008delinsGGT MANE Select	NP_000305.3:p.Tyr336Gly