Canonical Allele Identifier: CA891840163

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960895_87960896delinsTT , CM000672.2:g.87960895_87960896delinsTT	GRCh38
NC_000010.10:g.89720652_89720653delinsTT , CM000672.1:g.89720652_89720653delinsTT	GRCh37
NC_000010.9:g.89710632_89710633delinsTT	NCBI36
NG_007466.2:g.102457_102458delinsTT , LRG_311:g.102457_102458delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.896_897delinsTT	ENSP00000514759.2:p.Asp299Val
ENST00000710265.1:c.803_804delinsTT	ENSP00000518161.1:p.Asp268Val
ENST00000472832.3:c.803_804delinsTT	ENSP00000483066.2:p.Asp268Val
ENST00000688158.2:n.1538_1539delinsTT
ENST00000688922.2:c.*633_*634delinsTT	ENSP00000508742.2:n.*633_*634delinsTT
ENST00000700021.1:c.758_759delinsTT	ENSP00000514757.1:p.Asp253Val
ENST00000700022.1:c.*142_*143delinsTT	ENSP00000514758.1:n.*142_*143delinsTT
ENST00000700023.1:n.1961_1962delinsTT
ENST00000700024.1:n.2195_2196delinsTT
ENST00000700025.1:n.1572_1573delinsTT
ENST00000700026.1:n.440_441delinsTT
ENST00000700029.1:c.730_731delinsTT
ENST00000706954.1:c.803_804delinsTT	ENSP00000516674.1:p.Asp268Val
ENST00000706955.1:c.*838_*839delinsTT	ENSP00000516675.1:n.*838_*839delinsTT
ENST00000686459.1:c.*389_*390delinsTT	ENSP00000508909.1:n.*389_*390delinsTT
ENST00000688158.1:c.*914_*915delinsTT	ENSP00000509254.1:n.*914_*915delinsTT
ENST00000688308.1:c.803_804delinsTT	ENSP00000508752.1:p.Asp268Val
ENST00000688922.1:c.724_725delinsTT
ENST00000693560.1:c.1322_1323delinsTT	ENSP00000509861.1:p.Asp441Val
ENST00000371953.8:c.803_804delinsTT MANE Select	ENSP00000361021.3:p.Asp268Val
ENST00000371953.7:c.803_804delinsTT	ENSP00000361021.3:p.Asp268Val
ENST00000472832.2:c.230_231delinsTT	ENSP00000483066.1:p.Asp77Val
NM_000314.5:c.803_804delinsTT	NP_000305.3:p.Asp268Val
NM_000314.6:c.803_804delinsTT	NP_000305.3:p.Asp268Val
NM_001304717.2:c.1322_1323delinsTT	NP_001291646.2:p.Asp441Val
NM_001304718.1:c.212_213delinsTT	NP_001291647.1:p.Asp71Val
XM_006717926.2:c.758_759delinsTT	XP_006717989.1:p.Asp253Val
XM_011539981.1:c.803_804delinsTT	XP_011538283.1:p.Asp268Val
XM_011539982.1:c.707_708delinsTT	XP_011538284.1:p.Asp236Val
XR_945791.1:n.1373_1374delinsTT
NM_000314.7:c.803_804delinsTT	NP_000305.3:p.Asp268Val
NM_001304717.5:c.1322_1323delinsTT	NP_001291646.4:p.Asp441Val
NM_001304718.2:c.212_213delinsTT	NP_001291647.1:p.Asp71Val
NM_000314.8:c.803_804delinsTT MANE Select	NP_000305.3:p.Asp268Val