Canonical Allele Identifier: CA470661825

Gene: PTEN

Linked Data

• COSMIC: COSM5843
• MyVariant Identifiers: chr10:g.89692903del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933146del , CM000672.2:g.87933146del	GRCh38
NC_000010.10:g.89692903del , CM000672.1:g.89692903del	GRCh37
NC_000010.9:g.89682883del	NCBI36
NG_007466.2:g.74708del , LRG_311:g.74708del

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.387del	ENSP00000514759.2:p.Arg130GlufsTer4
ENST00000710265.1:c.387del	ENSP00000518161.1:p.Arg130GlufsTer4
ENST00000472832.3:c.387del	ENSP00000483066.2:p.Arg130GlufsTer4
ENST00000688158.2:n.1122del
ENST00000688922.2:c.*217del	ENSP00000508742.2:n.*217del
ENST00000700021.1:c.342del	ENSP00000514757.1:p.Arg115GlufsTer4
ENST00000700022.1:c.387del	ENSP00000514758.1:p.Arg130GlufsTer4
ENST00000700029.1:c.221del
ENST00000706954.1:c.387del	ENSP00000516674.1:p.Arg130GlufsTer4
ENST00000706955.1:c.*422del	ENSP00000516675.1:n.*422del
ENST00000686459.1:c.387del	ENSP00000508909.1:p.Arg130GlufsTer4
ENST00000688158.1:c.*498del	ENSP00000509254.1:n.*498del
ENST00000688308.1:c.387del	ENSP00000508752.1:p.Arg130GlufsTer4
ENST00000688922.1:c.308del
ENST00000693560.1:c.906del	ENSP00000509861.1:p.Arg303GlufsTer4
ENST00000371953.8:c.387del MANE Select	ENSP00000361021.3:p.Arg130GlufsTer4
ENST00000371953.7:c.387del	ENSP00000361021.3:p.Arg130GlufsTer4
ENST00000498703.1:n.213del
ENST00000610634.1:c.285del	ENSP00000477517.1:p.Arg96GlufsTer4
NM_000314.5:c.387del	NP_000305.3:p.Arg130GlufsTer4
NM_000314.6:c.387del	NP_000305.3:p.Arg130GlufsTer4
NM_001304717.2:c.906del	NP_001291646.2:p.Arg303GlufsTer4
NM_001304718.1:c.-364del	NP_001291647.1:n.-364del
XM_006717926.2:c.342del	XP_006717989.1:p.Arg115GlufsTer4
XM_011539981.1:c.387del	XP_011538283.1:p.Arg130GlufsTer4
XM_011539982.1:c.291del	XP_011538284.1:p.Arg98GlufsTer4
XR_945789.1:n.1099del
XR_945790.1:n.1099del
XR_945791.1:n.1099del
NM_000314.7:c.387del	NP_000305.3:p.Arg130GlufsTer4
NM_001304717.5:c.906del	NP_001291646.4:p.Arg303GlufsTer4
NM_001304718.2:c.-364del	NP_001291647.1:n.-364del
NM_000314.8:c.387del MANE Select	NP_000305.3:p.Arg130GlufsTer4