Canonical Allele Identifier: CA2579926759

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960915_87960917delinsTCT , CM000672.2:g.87960915_87960917delinsTCT	GRCh38
NC_000010.10:g.89720672_89720674delinsTCT , CM000672.1:g.89720672_89720674delinsTCT	GRCh37
NC_000010.9:g.89710652_89710654delinsTCT	NCBI36
NG_007466.2:g.102477_102479delinsTCT , LRG_311:g.102477_102479delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.916_918delinsTCT	ENSP00000514759.2:p.Val306Ser
ENST00000710265.1:c.823_825delinsTCT	ENSP00000518161.1:p.Val275Ser
ENST00000472832.3:c.823_825delinsTCT	ENSP00000483066.2:p.Val275Ser
ENST00000688158.2:n.1558_1560delinsTCT
ENST00000688922.2:c.*653_*655delinsTCT	ENSP00000508742.2:n.*653_*655delinsTCT
ENST00000700021.1:c.778_780delinsTCT	ENSP00000514757.1:p.Val260Ser
ENST00000700022.1:c.*162_*164delinsTCT	ENSP00000514758.1:n.*162_*164delinsTCT
ENST00000700023.1:n.1981_1983delinsTCT
ENST00000700024.1:n.2215_2217delinsTCT
ENST00000700025.1:n.1592_1594delinsTCT
ENST00000700026.1:n.460_462delinsTCT
ENST00000700029.1:c.750_752delinsTCT
ENST00000706954.1:c.823_825delinsTCT	ENSP00000516674.1:p.Val275Ser
ENST00000706955.1:c.*858_*860delinsTCT	ENSP00000516675.1:n.*858_*860delinsTCT
ENST00000686459.1:c.*409_*411delinsTCT	ENSP00000508909.1:n.*409_*411delinsTCT
ENST00000688158.1:c.*934_*936delinsTCT	ENSP00000509254.1:n.*934_*936delinsTCT
ENST00000688308.1:c.823_825delinsTCT	ENSP00000508752.1:p.Val275Ser
ENST00000688922.1:c.744_746delinsTCT
ENST00000693560.1:c.1342_1344delinsTCT	ENSP00000509861.1:p.Val448Ser
ENST00000371953.8:c.823_825delinsTCT MANE Select	ENSP00000361021.3:p.Val275Ser
ENST00000371953.7:c.823_825delinsTCT	ENSP00000361021.3:p.Val275Ser
ENST00000472832.2:c.250_252delinsTCT	ENSP00000483066.1:p.Val84Ser
NM_000314.5:c.823_825delinsTCT	NP_000305.3:p.Val275Ser
NM_000314.6:c.823_825delinsTCT	NP_000305.3:p.Val275Ser
NM_001304717.2:c.1342_1344delinsTCT	NP_001291646.2:p.Val448Ser
NM_001304718.1:c.232_234delinsTCT	NP_001291647.1:p.Val78Ser
XM_006717926.2:c.778_780delinsTCT	XP_006717989.1:p.Val260Ser
XM_011539981.1:c.823_825delinsTCT	XP_011538283.1:p.Val275Ser
XM_011539982.1:c.727_729delinsTCT	XP_011538284.1:p.Val243Ser
XR_945791.1:n.1393_1395delinsTCT
NM_000314.7:c.823_825delinsTCT	NP_000305.3:p.Val275Ser
NM_001304717.5:c.1342_1344delinsTCT	NP_001291646.4:p.Val448Ser
NM_001304718.2:c.232_234delinsTCT	NP_001291647.1:p.Val78Ser
NM_000314.8:c.823_825delinsTCT MANE Select	NP_000305.3:p.Val275Ser