Canonical Allele Identifier: CA1926190121

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961100_87961101delinsCT , CM000672.2:g.87961100_87961101delinsCT	GRCh38
NC_000010.10:g.89720857_89720858delinsCT , CM000672.1:g.89720857_89720858delinsCT	GRCh37
NC_000010.9:g.89710837_89710838delinsCT	NCBI36
NG_007466.2:g.102662_102663delinsCT , LRG_311:g.102662_102663delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1101_1102delinsCT	ENSP00000514759.2:p.Tyr367=
ENST00000710265.1:c.1008_1009delinsCT	ENSP00000518161.1:p.Tyr336=
ENST00000472832.3:c.1008_1009delinsCT	ENSP00000483066.2:p.Tyr336=
ENST00000688158.2:n.1743_1744delinsCT
ENST00000688922.2:c.*838_*839delinsCT	ENSP00000508742.2:n.*838_*839delinsCT
ENST00000700021.1:c.963_964delinsCT	ENSP00000514757.1:p.Tyr321=
ENST00000700022.1:c.*347_*348delinsCT	ENSP00000514758.1:n.*347_*348delinsCT
ENST00000700023.1:n.2166_2167delinsCT
ENST00000700024.1:n.2400_2401delinsCT
ENST00000700025.1:n.1777_1778delinsCT
ENST00000700026.1:n.645_646delinsCT
ENST00000706954.1:c.1008_1009delinsCT	ENSP00000516674.1:p.Tyr336=
ENST00000706955.1:c.*1043_*1044delinsCT	ENSP00000516675.1:n.*1043_*1044delinsCT
ENST00000686459.1:c.*594_*595delinsCT	ENSP00000508909.1:n.*594_*595delinsCT
ENST00000688158.1:c.*1119_*1120delinsCT	ENSP00000509254.1:n.*1119_*1120delinsCT
ENST00000688308.1:c.1008_1009delinsCT	ENSP00000508752.1:p.Tyr336=
ENST00000688922.1:c.929_930delinsCT
ENST00000693560.1:c.1527_1528delinsCT	ENSP00000509861.1:p.Tyr509=
ENST00000371953.8:c.1008_1009delinsCT MANE Select	ENSP00000361021.3:p.Tyr336=
ENST00000371953.7:c.1008_1009delinsCT	ENSP00000361021.3:p.Tyr336=
ENST00000472832.2:c.435_436delinsCT	ENSP00000483066.1:p.Tyr145=
NM_000314.5:c.1008_1009delinsCT	NP_000305.3:p.Tyr336=
NM_000314.6:c.1008_1009delinsCT	NP_000305.3:p.Tyr336=
NM_001304717.2:c.1527_1528delinsCT	NP_001291646.2:p.Tyr509=
NM_001304718.1:c.417_418delinsCT	NP_001291647.1:p.Tyr139=
XM_006717926.2:c.963_964delinsCT	XP_006717989.1:p.Tyr321=
XM_011539981.1:c.1008_1009delinsCT	XP_011538283.1:p.Tyr336=
XM_011539982.1:c.912_913delinsCT	XP_011538284.1:p.Tyr304=
XR_945791.1:n.1578_1579delinsCT
NM_000314.7:c.1008_1009delinsCT	NP_000305.3:p.Tyr336=
NM_001304717.5:c.1527_1528delinsCT	NP_001291646.4:p.Tyr509=
NM_001304718.2:c.417_418delinsCT	NP_001291647.1:p.Tyr139=
NM_000314.8:c.1008_1009delinsCT MANE Select	NP_000305.3:p.Tyr336=