Canonical Allele Identifier: CA16613156

Gene: PTEN

Linked Data

• ClinVar Variation Id: 412801
• ClinVar RCV Id: RCV000464638 ; RCV000482827 ; RCV000580574
• dbSNP Id: rs1060503841

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925566_87925567delinsCC , CM000672.2:g.87925566_87925567delinsCC	GRCh38
NC_000010.10:g.89685323_89685324delinsCC , CM000672.1:g.89685323_89685324delinsCC	GRCh37
NC_000010.9:g.89675303_89675304delinsCC	NCBI36
NG_007466.2:g.67128_67129delinsCC , LRG_311:g.67128_67129delinsCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.209+9_209+10delinsCC	ENSP00000514759.2:n.209+9_209+10delinsCC
ENST00000710265.1:c.209+9_209+10delinsCC	ENSP00000518161.1:n.209+9_209+10delinsCC
ENST00000472832.3:c.209+9_209+10delinsCC	ENSP00000483066.2:n.209+9_209+10delinsCC
ENST00000688158.2:n.944+9_944+10delinsCC
ENST00000688922.2:c.209+9_209+10delinsCC	ENSP00000508742.2:n.209+9_209+10delinsCC
ENST00000700021.1:c.165-5480_165-5479delinsCC	ENSP00000514757.1:n.165-5480_165-5479deli...
ENST00000700022.1:c.209+9_209+10delinsCC	ENSP00000514758.1:n.209+9_209+10delinsCC
ENST00000700029.1:c.43+9_43+10delinsCC
ENST00000706954.1:c.209+9_209+10delinsCC	ENSP00000516674.1:n.209+9_209+10delinsCC
ENST00000706955.1:c.*244+9_*244+10delinsCC	ENSP00000516675.1:n.*244+9_*244+10delinsC...
ENST00000686459.1:c.209+9_209+10delinsCC	ENSP00000508909.1:n.209+9_209+10delinsCC
ENST00000688158.1:c.*320+9_*320+10delinsCC	ENSP00000509254.1:n.*320+9_*320+10delinsC...
ENST00000688308.1:c.209+9_209+10delinsCC	ENSP00000508752.1:n.209+9_209+10delinsCC
ENST00000688922.1:c.78+9_78+10delinsCC
ENST00000693560.1:c.728+9_728+10delinsCC	ENSP00000509861.1:n.728+9_728+10delinsCC
ENST00000371953.8:c.209+9_209+10delinsCC MANE Select	ENSP00000361021.3:n.209+9_209+10delinsCC
ENST00000371953.7:c.209+9_209+10delinsCC	ENSP00000361021.3:n.209+9_209+10delinsCC
ENST00000498703.1:n.35+9_35+10delinsCC
ENST00000610634.1:c.107+9_107+10delinsCC	ENSP00000477517.1:n.107+9_107+10delinsCC
NM_000314.5:c.209+9_209+10delinsCC	NP_000305.3:n.209+9_209+10delinsCC
NM_000314.6:c.209+9_209+10delinsCC	NP_000305.3:n.209+9_209+10delinsCC
NM_001304717.2:c.728+9_728+10delinsCC	NP_001291646.2:n.728+9_728+10delinsCC
NM_001304718.1:c.-541-5480_-541-5479delinsCC	NP_001291647.1:n.-541-5480_-541-5479delin...
XM_006717926.2:c.165-5480_165-5479delinsCC	XP_006717989.1:n.165-5480_165-5479delinsC...
XM_011539981.1:c.209+9_209+10delinsCC	XP_011538283.1:n.209+9_209+10delinsCC
XM_011539982.1:c.113+9_113+10delinsCC	XP_011538284.1:n.113+9_113+10delinsCC
XR_945789.1:n.921+9_921+10delinsCC
XR_945790.1:n.921+9_921+10delinsCC
XR_945791.1:n.921+9_921+10delinsCC
NM_000314.7:c.209+9_209+10delinsCC	NP_000305.3:n.209+9_209+10delinsCC
NM_001304717.5:c.728+9_728+10delinsCC	NP_001291646.4:n.728+9_728+10delinsCC
NM_001304718.2:c.-541-5480_-541-5479delinsCC	NP_001291647.1:n.-541-5480_-541-5479delin...
NM_000314.8:c.209+9_209+10delinsCC MANE Select	NP_000305.3:n.209+9_209+10delinsCC