Canonical Allele Identifier: CA2579927131

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894042_87894043delinsTA , CM000672.2:g.87894042_87894043delinsTA	GRCh38
NC_000010.10:g.89653799_89653800delinsTA , CM000672.1:g.89653799_89653800delinsTA	GRCh37
NC_000010.9:g.89643779_89643780delinsTA	NCBI36
NG_007466.2:g.35604_35605delinsTA , LRG_311:g.35604_35605delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.97_98delinsTA	ENSP00000514759.2:p.Ile33Tyr
ENST00000710265.1:c.97_98delinsTA	ENSP00000518161.1:p.Ile33Tyr
ENST00000472832.3:c.97_98delinsTA	ENSP00000483066.2:p.Ile33Tyr
ENST00000688158.2:n.899+13604_899+13605delinsTA
ENST00000688922.2:c.97_98delinsTA	ENSP00000508742.2:p.Ile33Tyr
ENST00000700021.1:c.97_98delinsTA	ENSP00000514757.1:p.Ile33Tyr
ENST00000700022.1:c.97_98delinsTA	ENSP00000514758.1:p.Ile33Tyr
ENST00000706954.1:c.97_98delinsTA	ENSP00000516674.1:p.Ile33Tyr
ENST00000706955.1:c.*132_*133delinsTA	ENSP00000516675.1:n.*132_*133delinsTA
ENST00000686459.1:c.97_98delinsTA	ENSP00000508909.1:p.Ile33Tyr
ENST00000688158.1:c.*275+13604_*275+13605delinsTA	ENSP00000509254.1:n.*275+13604_*275+13605delinsTA
ENST00000688308.1:c.97_98delinsTA	ENSP00000508752.1:p.Ile33Tyr
ENST00000693560.1:c.616_617delinsTA	ENSP00000509861.1:p.Ile206Tyr
ENST00000371953.8:c.97_98delinsTA MANE Select	ENSP00000361021.3:p.Ile33Tyr
ENST00000371953.7:c.97_98delinsTA	ENSP00000361021.3:p.Ile33Tyr
ENST00000462694.1:n.99_100delinsTA
ENST00000610634.1:c.-6_-5delinsTA	ENSP00000477517.1:n.-6_-5delinsTA
NM_000314.5:c.97_98delinsTA	NP_000305.3:p.Ile33Tyr
NM_000314.6:c.97_98delinsTA	NP_000305.3:p.Ile33Tyr
NM_001304717.2:c.616_617delinsTA	NP_001291646.2:p.Ile206Tyr
NM_001304718.1:c.-609_-608delinsTA	NP_001291647.1:n.-609_-608delinsTA
XM_006717926.2:c.97_98delinsTA	XP_006717989.1:p.Ile33Tyr
XM_011539981.1:c.97_98delinsTA	XP_011538283.1:p.Ile33Tyr
XM_011539982.1:c.68+13604_68+13605delinsTA	XP_011538284.1:n.68+13604_68+13605delinsTA
XR_945789.1:n.809_810delinsTA
XR_945790.1:n.809_810delinsTA
XR_945791.1:n.809_810delinsTA
NM_000314.7:c.97_98delinsTA	NP_000305.3:p.Ile33Tyr
NM_001304717.5:c.616_617delinsTA	NP_001291646.4:p.Ile206Tyr
NM_001304718.2:c.-609_-608delinsTA	NP_001291647.1:n.-609_-608delinsTA
NM_000314.8:c.97_98delinsTA MANE Select	NP_000305.3:p.Ile33Tyr