Canonical Allele Identifier: CA891841406

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961098_87961099delinsGC , CM000672.2:g.87961098_87961099delinsGC	GRCh38
NC_000010.10:g.89720855_89720856delinsGC , CM000672.1:g.89720855_89720856delinsGC	GRCh37
NC_000010.9:g.89710835_89710836delinsGC	NCBI36
NG_007466.2:g.102660_102661delinsGC , LRG_311:g.102660_102661delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1099_1100delinsGC	ENSP00000514759.2:p.Tyr367Ala
ENST00000710265.1:c.1006_1007delinsGC	ENSP00000518161.1:p.Tyr336Ala
ENST00000472832.3:c.1006_1007delinsGC	ENSP00000483066.2:p.Tyr336Ala
ENST00000688158.2:n.1741_1742delinsGC
ENST00000688922.2:c.*836_*837delinsGC	ENSP00000508742.2:n.*836_*837delinsGC
ENST00000700021.1:c.961_962delinsGC	ENSP00000514757.1:p.Tyr321Ala
ENST00000700022.1:c.*345_*346delinsGC	ENSP00000514758.1:n.*345_*346delinsGC
ENST00000700023.1:n.2164_2165delinsGC
ENST00000700024.1:n.2398_2399delinsGC
ENST00000700025.1:n.1775_1776delinsGC
ENST00000700026.1:n.643_644delinsGC
ENST00000706954.1:c.1006_1007delinsGC	ENSP00000516674.1:p.Tyr336Ala
ENST00000706955.1:c.*1041_*1042delinsGC	ENSP00000516675.1:n.*1041_*1042delinsGC
ENST00000686459.1:c.*592_*593delinsGC	ENSP00000508909.1:n.*592_*593delinsGC
ENST00000688158.1:c.*1117_*1118delinsGC	ENSP00000509254.1:n.*1117_*1118delinsGC
ENST00000688308.1:c.1006_1007delinsGC	ENSP00000508752.1:p.Tyr336Ala
ENST00000688922.1:c.927_928delinsGC
ENST00000693560.1:c.1525_1526delinsGC	ENSP00000509861.1:p.Tyr509Ala
ENST00000371953.8:c.1006_1007delinsGC MANE Select	ENSP00000361021.3:p.Tyr336Ala
ENST00000371953.7:c.1006_1007delinsGC	ENSP00000361021.3:p.Tyr336Ala
ENST00000472832.2:c.433_434delinsGC	ENSP00000483066.1:p.Tyr145Ala
NM_000314.5:c.1006_1007delinsGC	NP_000305.3:p.Tyr336Ala
NM_000314.6:c.1006_1007delinsGC	NP_000305.3:p.Tyr336Ala
NM_001304717.2:c.1525_1526delinsGC	NP_001291646.2:p.Tyr509Ala
NM_001304718.1:c.415_416delinsGC	NP_001291647.1:p.Tyr139Ala
XM_006717926.2:c.961_962delinsGC	XP_006717989.1:p.Tyr321Ala
XM_011539981.1:c.1006_1007delinsGC	XP_011538283.1:p.Tyr336Ala
XM_011539982.1:c.910_911delinsGC	XP_011538284.1:p.Tyr304Ala
XR_945791.1:n.1576_1577delinsGC
NM_000314.7:c.1006_1007delinsGC	NP_000305.3:p.Tyr336Ala
NM_001304717.5:c.1525_1526delinsGC	NP_001291646.4:p.Tyr509Ala
NM_001304718.2:c.415_416delinsGC	NP_001291647.1:p.Tyr139Ala
NM_000314.8:c.1006_1007delinsGC MANE Select	NP_000305.3:p.Tyr336Ala