Canonical Allele Identifier: CA891837648

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933144_87933146delinsTAT , CM000672.2:g.87933144_87933146delinsTAT	GRCh38
NC_000010.10:g.89692901_89692903delinsTAT , CM000672.1:g.89692901_89692903delinsTAT	GRCh37
NC_000010.9:g.89682881_89682883delinsTAT	NCBI36
NG_007466.2:g.74706_74708delinsTAT , LRG_311:g.74706_74708delinsTAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.385_387delinsTAT	ENSP00000514759.2:p.Gly129Tyr
ENST00000710265.1:c.385_387delinsTAT	ENSP00000518161.1:p.Gly129Tyr
ENST00000472832.3:c.385_387delinsTAT	ENSP00000483066.2:p.Gly129Tyr
ENST00000688158.2:n.1120_1122delinsTAT
ENST00000688922.2:c.*215_*217delinsTAT	ENSP00000508742.2:n.*215_*217delinsTAT
ENST00000700021.1:c.340_342delinsTAT	ENSP00000514757.1:p.Gly114Tyr
ENST00000700022.1:c.385_387delinsTAT	ENSP00000514758.1:p.Gly129Tyr
ENST00000700029.1:c.219_221delinsTAT
ENST00000706954.1:c.385_387delinsTAT	ENSP00000516674.1:p.Gly129Tyr
ENST00000706955.1:c.*420_*422delinsTAT	ENSP00000516675.1:n.*420_*422delinsTAT
ENST00000686459.1:c.385_387delinsTAT	ENSP00000508909.1:p.Gly129Tyr
ENST00000688158.1:c.*496_*498delinsTAT	ENSP00000509254.1:n.*496_*498delinsTAT
ENST00000688308.1:c.385_387delinsTAT	ENSP00000508752.1:p.Gly129Tyr
ENST00000688922.1:c.306_308delinsTAT
ENST00000693560.1:c.904_906delinsTAT	ENSP00000509861.1:p.Gly302Tyr
ENST00000371953.8:c.385_387delinsTAT MANE Select	ENSP00000361021.3:p.Gly129Tyr
ENST00000371953.7:c.385_387delinsTAT	ENSP00000361021.3:p.Gly129Tyr
ENST00000498703.1:n.211_213delinsTAT
ENST00000610634.1:c.283_285delinsTAT	ENSP00000477517.1:p.Gly95Tyr
NM_000314.5:c.385_387delinsTAT	NP_000305.3:p.Gly129Tyr
NM_000314.6:c.385_387delinsTAT	NP_000305.3:p.Gly129Tyr
NM_001304717.2:c.904_906delinsTAT	NP_001291646.2:p.Gly302Tyr
NM_001304718.1:c.-366_-364delinsTAT	NP_001291647.1:n.-366_-364delinsTAT
XM_006717926.2:c.340_342delinsTAT	XP_006717989.1:p.Gly114Tyr
XM_011539981.1:c.385_387delinsTAT	XP_011538283.1:p.Gly129Tyr
XM_011539982.1:c.289_291delinsTAT	XP_011538284.1:p.Gly97Tyr
XR_945789.1:n.1097_1099delinsTAT
XR_945790.1:n.1097_1099delinsTAT
XR_945791.1:n.1097_1099delinsTAT
NM_000314.7:c.385_387delinsTAT	NP_000305.3:p.Gly129Tyr
NM_001304717.5:c.904_906delinsTAT	NP_001291646.4:p.Gly302Tyr
NM_001304718.2:c.-366_-364delinsTAT	NP_001291647.1:n.-366_-364delinsTAT
NM_000314.8:c.385_387delinsTAT MANE Select	NP_000305.3:p.Gly129Tyr