Canonical Allele Identifier: CA645553801

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933059_87933090dup , CM000672.2:g.87933059_87933090dup	GRCh38
NC_000010.10:g.89692816_89692847dup , CM000672.1:g.89692816_89692847dup	GRCh37
NC_000010.9:g.89682796_89682827dup	NCBI36
NG_007466.2:g.74621_74652dup , LRG_311:g.74621_74652dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.300_331dup	ENSP00000514759.2:p.Trp111LeufsTer13
ENST00000710265.1:c.300_331dup	ENSP00000518161.1:p.Trp111LeufsTer13
ENST00000472832.3:c.300_331dup	ENSP00000483066.2:p.Trp111LeufsTer13
ENST00000688158.2:n.1035_1066dup
ENST00000688922.2:c.*130_*161dup	ENSP00000508742.2:n.*130_*161dup
ENST00000700021.1:c.255_286dup	ENSP00000514757.1:p.Trp96LeufsTer13
ENST00000700022.1:c.300_331dup	ENSP00000514758.1:p.Trp111LeufsTer13
ENST00000700029.1:c.134_165dup
ENST00000706954.1:c.300_331dup	ENSP00000516674.1:p.Trp111LeufsTer13
ENST00000706955.1:c.*335_*366dup	ENSP00000516675.1:n.*335_*366dup
ENST00000686459.1:c.300_331dup	ENSP00000508909.1:p.Trp111LeufsTer13
ENST00000688158.1:c.*411_*442dup	ENSP00000509254.1:n.*411_*442dup
ENST00000688308.1:c.300_331dup	ENSP00000508752.1:p.Trp111LeufsTer13
ENST00000688922.1:c.221_252dup
ENST00000693560.1:c.819_850dup	ENSP00000509861.1:p.Trp284LeufsTer13
ENST00000371953.8:c.300_331dup MANE Select	ENSP00000361021.3:p.Trp111LeufsTer13
ENST00000371953.7:c.300_331dup	ENSP00000361021.3:p.Trp111LeufsTer13
ENST00000498703.1:n.126_157dup
ENST00000610634.1:c.198_229dup	ENSP00000477517.1:p.Trp77LeufsTer13
NM_000314.5:c.300_331dup	NP_000305.3:p.Trp111LeufsTer13
NM_000314.6:c.300_331dup	NP_000305.3:p.Trp111LeufsTer13
NM_001304717.2:c.819_850dup	NP_001291646.2:p.Trp284LeufsTer13
NM_001304718.1:c.-451_-420dup	NP_001291647.1:n.-451_-420dup
XM_006717926.2:c.255_286dup	XP_006717989.1:p.Trp96LeufsTer13
XM_011539981.1:c.300_331dup	XP_011538283.1:p.Trp111LeufsTer13
XM_011539982.1:c.204_235dup	XP_011538284.1:p.Trp79LeufsTer13
XR_945789.1:n.1012_1043dup
XR_945790.1:n.1012_1043dup
XR_945791.1:n.1012_1043dup
NM_000314.7:c.300_331dup	NP_000305.3:p.Trp111LeufsTer13
NM_001304717.5:c.819_850dup	NP_001291646.4:p.Trp284LeufsTer13
NM_001304718.2:c.-451_-420dup	NP_001291647.1:n.-451_-420dup
NM_000314.8:c.300_331dup MANE Select	NP_000305.3:p.Trp111LeufsTer13