Canonical Allele Identifier: CA891840164

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960895_87960896delinsCT , CM000672.2:g.87960895_87960896delinsCT	GRCh38
NC_000010.10:g.89720652_89720653delinsCT , CM000672.1:g.89720652_89720653delinsCT	GRCh37
NC_000010.9:g.89710632_89710633delinsCT	NCBI36
NG_007466.2:g.102457_102458delinsCT , LRG_311:g.102457_102458delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.896_897delinsCT	ENSP00000514759.2:p.Asp299Ala
ENST00000710265.1:c.803_804delinsCT	ENSP00000518161.1:p.Asp268Ala
ENST00000472832.3:c.803_804delinsCT	ENSP00000483066.2:p.Asp268Ala
ENST00000688158.2:n.1538_1539delinsCT
ENST00000688922.2:c.*633_*634delinsCT	ENSP00000508742.2:n.*633_*634delinsCT
ENST00000700021.1:c.758_759delinsCT	ENSP00000514757.1:p.Asp253Ala
ENST00000700022.1:c.*142_*143delinsCT	ENSP00000514758.1:n.*142_*143delinsCT
ENST00000700023.1:n.1961_1962delinsCT
ENST00000700024.1:n.2195_2196delinsCT
ENST00000700025.1:n.1572_1573delinsCT
ENST00000700026.1:n.440_441delinsCT
ENST00000700029.1:c.730_731delinsCT
ENST00000706954.1:c.803_804delinsCT	ENSP00000516674.1:p.Asp268Ala
ENST00000706955.1:c.*838_*839delinsCT	ENSP00000516675.1:n.*838_*839delinsCT
ENST00000686459.1:c.*389_*390delinsCT	ENSP00000508909.1:n.*389_*390delinsCT
ENST00000688158.1:c.*914_*915delinsCT	ENSP00000509254.1:n.*914_*915delinsCT
ENST00000688308.1:c.803_804delinsCT	ENSP00000508752.1:p.Asp268Ala
ENST00000688922.1:c.724_725delinsCT
ENST00000693560.1:c.1322_1323delinsCT	ENSP00000509861.1:p.Asp441Ala
ENST00000371953.8:c.803_804delinsCT MANE Select	ENSP00000361021.3:p.Asp268Ala
ENST00000371953.7:c.803_804delinsCT	ENSP00000361021.3:p.Asp268Ala
ENST00000472832.2:c.230_231delinsCT	ENSP00000483066.1:p.Asp77Ala
NM_000314.5:c.803_804delinsCT	NP_000305.3:p.Asp268Ala
NM_000314.6:c.803_804delinsCT	NP_000305.3:p.Asp268Ala
NM_001304717.2:c.1322_1323delinsCT	NP_001291646.2:p.Asp441Ala
NM_001304718.1:c.212_213delinsCT	NP_001291647.1:p.Asp71Ala
XM_006717926.2:c.758_759delinsCT	XP_006717989.1:p.Asp253Ala
XM_011539981.1:c.803_804delinsCT	XP_011538283.1:p.Asp268Ala
XM_011539982.1:c.707_708delinsCT	XP_011538284.1:p.Asp236Ala
XR_945791.1:n.1373_1374delinsCT
NM_000314.7:c.803_804delinsCT	NP_000305.3:p.Asp268Ala
NM_001304717.5:c.1322_1323delinsCT	NP_001291646.4:p.Asp441Ala
NM_001304718.2:c.212_213delinsCT	NP_001291647.1:p.Asp71Ala
NM_000314.8:c.803_804delinsCT MANE Select	NP_000305.3:p.Asp268Ala