Canonical Allele Identifier: CA2695200976

Gene: PTEN

Linked Data

• ClinVar Variation Id: 2674338
• ClinVar RCV Id: RCV003452534

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894110_87894118delinsTTAC , CM000672.2:g.87894110_87894118delinsTTAC	GRCh38
NC_000010.10:g.89653867_89653875delinsTTAC , CM000672.1:g.89653867_89653875delinsTTAC	GRCh37
NC_000010.9:g.89643847_89643855delinsTTAC	NCBI36
NG_007466.2:g.35672_35680delinsTTAC , LRG_311:g.35672_35680delinsTTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.164+1_164+9delinsTTAC	ENSP00000514759.2:n.164+1_164+9delinsTTAC
ENST00000710265.1:c.164+1_164+9delinsTTAC	ENSP00000518161.1:n.164+1_164+9delinsTTAC
ENST00000472832.3:c.164+1_164+9delinsTTAC	ENSP00000483066.2:n.164+1_164+9delinsTTAC
ENST00000688158.2:n.899+13672_899+13680delinsTTAC
ENST00000688922.2:c.164+1_164+9delinsTTAC	ENSP00000508742.2:n.164+1_164+9delinsTTAC
ENST00000700021.1:c.164+1_164+9delinsTTAC	ENSP00000514757.1:n.164+1_164+9delinsTTAC
ENST00000700022.1:c.164+1_164+9delinsTTAC	ENSP00000514758.1:n.164+1_164+9delinsTTAC
ENST00000706954.1:c.164+1_164+9delinsTTAC	ENSP00000516674.1:n.164+1_164+9delinsTTAC
ENST00000706955.1:c.*199+1_*199+9delinsTTAC	ENSP00000516675.1:n.*199+1_*199+9delinsTTAC
ENST00000686459.1:c.164+1_164+9delinsTTAC	ENSP00000508909.1:n.164+1_164+9delinsTTAC
ENST00000688158.1:c.*275+13672_*275+13680delinsTTAC	ENSP00000509254.1:n.*275+13672_*275+13680delinsTTAC
ENST00000688308.1:c.164+1_164+9delinsTTAC	ENSP00000508752.1:n.164+1_164+9delinsTTAC
ENST00000688922.1:c.33+1_33+9delinsTTAC
ENST00000693560.1:c.683+1_683+9delinsTTAC	ENSP00000509861.1:n.683+1_683+9delinsTTAC
ENST00000371953.8:c.164+1_164+9delinsTTAC MANE Select	ENSP00000361021.3:n.164+1_164+9delinsTTAC
ENST00000371953.7:c.164+1_164+9delinsTTAC	ENSP00000361021.3:n.164+1_164+9delinsTTAC
ENST00000462694.1:n.167_175delinsTTAC
ENST00000610634.1:c.62+1_62+9delinsTTAC	ENSP00000477517.1:n.62+1_62+9delinsTTAC
NM_000314.5:c.164+1_164+9delinsTTAC	NP_000305.3:n.164+1_164+9delinsTTAC
NM_000314.6:c.164+1_164+9delinsTTAC	NP_000305.3:n.164+1_164+9delinsTTAC
NM_001304717.2:c.683+1_683+9delinsTTAC	NP_001291646.2:n.683+1_683+9delinsTTAC
NM_001304718.1:c.-542+1_-542+9delinsTTAC	NP_001291647.1:n.-542+1_-542+9delinsTTAC
XM_006717926.2:c.164+1_164+9delinsTTAC	XP_006717989.1:n.164+1_164+9delinsTTAC
XM_011539981.1:c.164+1_164+9delinsTTAC	XP_011538283.1:n.164+1_164+9delinsTTAC
XM_011539982.1:c.68+13672_68+13680delinsTTAC	XP_011538284.1:n.68+13672_68+13680delinsTTAC
XR_945789.1:n.876+1_876+9delinsTTAC
XR_945790.1:n.876+1_876+9delinsTTAC
XR_945791.1:n.876+1_876+9delinsTTAC
NM_000314.7:c.164+1_164+9delinsTTAC	NP_000305.3:n.164+1_164+9delinsTTAC
NM_001304717.5:c.683+1_683+9delinsTTAC	NP_001291646.4:n.683+1_683+9delinsTTAC
NM_001304718.2:c.-542+1_-542+9delinsTTAC	NP_001291647.1:n.-542+1_-542+9delinsTTAC
NM_000314.8:c.164+1_164+9delinsTTAC MANE Select	NP_000305.3:n.164+1_164+9delinsTTAC