Canonical Allele Identifier: CA1926174357

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933068_87933069delinsCT , CM000672.2:g.87933068_87933069delinsCT	GRCh38
NC_000010.10:g.89692825_89692826delinsCT , CM000672.1:g.89692825_89692826delinsCT	GRCh37
NC_000010.9:g.89682805_89682806delinsCT	NCBI36
NG_007466.2:g.74630_74631delinsCT , LRG_311:g.74630_74631delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.309_310delinsCT	ENSP00000514759.2:p.Pro103=
ENST00000710265.1:c.309_310delinsCT	ENSP00000518161.1:p.Pro103=
ENST00000472832.3:c.309_310delinsCT	ENSP00000483066.2:p.Pro103=
ENST00000688158.2:n.1044_1045delinsCT
ENST00000688922.2:c.*139_*140delinsCT	ENSP00000508742.2:n.*139_*140delinsCT
ENST00000700021.1:c.264_265delinsCT	ENSP00000514757.1:p.Pro88=
ENST00000700022.1:c.309_310delinsCT	ENSP00000514758.1:p.Pro103=
ENST00000700029.1:c.143_144delinsCT
ENST00000706954.1:c.309_310delinsCT	ENSP00000516674.1:p.Pro103=
ENST00000706955.1:c.*344_*345delinsCT	ENSP00000516675.1:n.*344_*345delinsCT
ENST00000686459.1:c.309_310delinsCT	ENSP00000508909.1:p.Pro103=
ENST00000688158.1:c.*420_*421delinsCT	ENSP00000509254.1:n.*420_*421delinsCT
ENST00000688308.1:c.309_310delinsCT	ENSP00000508752.1:p.Pro103=
ENST00000688922.1:c.230_231delinsCT
ENST00000693560.1:c.828_829delinsCT	ENSP00000509861.1:p.Pro276=
ENST00000371953.8:c.309_310delinsCT MANE Select	ENSP00000361021.3:p.Pro103=
ENST00000371953.7:c.309_310delinsCT	ENSP00000361021.3:p.Pro103=
ENST00000498703.1:n.135_136delinsCT
ENST00000610634.1:c.207_208delinsCT	ENSP00000477517.1:p.Pro69=
NM_000314.5:c.309_310delinsCT	NP_000305.3:p.Pro103=
NM_000314.6:c.309_310delinsCT	NP_000305.3:p.Pro103=
NM_001304717.2:c.828_829delinsCT	NP_001291646.2:p.Pro276=
NM_001304718.1:c.-442_-441delinsCT	NP_001291647.1:n.-442_-441delinsCT
XM_006717926.2:c.264_265delinsCT	XP_006717989.1:p.Pro88=
XM_011539981.1:c.309_310delinsCT	XP_011538283.1:p.Pro103=
XM_011539982.1:c.213_214delinsCT	XP_011538284.1:p.Pro71=
XR_945789.1:n.1021_1022delinsCT
XR_945790.1:n.1021_1022delinsCT
XR_945791.1:n.1021_1022delinsCT
NM_000314.7:c.309_310delinsCT	NP_000305.3:p.Pro103=
NM_001304717.5:c.828_829delinsCT	NP_001291646.4:p.Pro276=
NM_001304718.2:c.-442_-441delinsCT	NP_001291647.1:n.-442_-441delinsCT
NM_000314.8:c.309_310delinsCT MANE Select	NP_000305.3:p.Pro103=