Canonical Allele Identifier: CA891835572

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894105_87894107delinsTCT , CM000672.2:g.87894105_87894107delinsTCT	GRCh38
NC_000010.10:g.89653862_89653864delinsTCT , CM000672.1:g.89653862_89653864delinsTCT	GRCh37
NC_000010.9:g.89643842_89643844delinsTCT	NCBI36
NG_007466.2:g.35667_35669delinsTCT , LRG_311:g.35667_35669delinsTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.160_162delinsTCT	ENSP00000514759.2:p.Val54Ser
ENST00000710265.1:c.160_162delinsTCT	ENSP00000518161.1:p.Val54Ser
ENST00000472832.3:c.160_162delinsTCT	ENSP00000483066.2:p.Val54Ser
ENST00000688158.2:n.899+13667_899+13669delinsTCT
ENST00000688922.2:c.160_162delinsTCT	ENSP00000508742.2:p.Val54Ser
ENST00000700021.1:c.160_162delinsTCT	ENSP00000514757.1:p.Val54Ser
ENST00000700022.1:c.160_162delinsTCT	ENSP00000514758.1:p.Val54Ser
ENST00000706954.1:c.160_162delinsTCT	ENSP00000516674.1:p.Val54Ser
ENST00000706955.1:c.*195_*197delinsTCT	ENSP00000516675.1:n.*195_*197delinsTCT
ENST00000686459.1:c.160_162delinsTCT	ENSP00000508909.1:p.Val54Ser
ENST00000688158.1:c.*275+13667_*275+13669delinsTCT	ENSP00000509254.1:n.*275+13667_*275+13669delinsTCT
ENST00000688308.1:c.160_162delinsTCT	ENSP00000508752.1:p.Val54Ser
ENST00000688922.1:c.29_31delinsTCT
ENST00000693560.1:c.679_681delinsTCT	ENSP00000509861.1:p.Val227Ser
ENST00000371953.8:c.160_162delinsTCT MANE Select	ENSP00000361021.3:p.Val54Ser
ENST00000371953.7:c.160_162delinsTCT	ENSP00000361021.3:p.Val54Ser
ENST00000462694.1:n.162_164delinsTCT
ENST00000610634.1:c.58_60delinsTCT	ENSP00000477517.1:p.Val20Ser
NM_000314.5:c.160_162delinsTCT	NP_000305.3:p.Val54Ser
NM_000314.6:c.160_162delinsTCT	NP_000305.3:p.Val54Ser
NM_001304717.2:c.679_681delinsTCT	NP_001291646.2:p.Val227Ser
NM_001304718.1:c.-546_-544delinsTCT	NP_001291647.1:n.-546_-544delinsTCT
XM_006717926.2:c.160_162delinsTCT	XP_006717989.1:p.Val54Ser
XM_011539981.1:c.160_162delinsTCT	XP_011538283.1:p.Val54Ser
XM_011539982.1:c.68+13667_68+13669delinsTCT	XP_011538284.1:n.68+13667_68+13669delinsTCT
XR_945789.1:n.872_874delinsTCT
XR_945790.1:n.872_874delinsTCT
XR_945791.1:n.872_874delinsTCT
NM_000314.7:c.160_162delinsTCT	NP_000305.3:p.Val54Ser
NM_001304717.5:c.679_681delinsTCT	NP_001291646.4:p.Val227Ser
NM_001304718.2:c.-546_-544delinsTCT	NP_001291647.1:n.-546_-544delinsTCT
NM_000314.8:c.160_162delinsTCT MANE Select	NP_000305.3:p.Val54Ser