Canonical Allele Identifier: CA891834550

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894030_87894031delinsAC , CM000672.2:g.87894030_87894031delinsAC	GRCh38
NC_000010.10:g.89653787_89653788delinsAC , CM000672.1:g.89653787_89653788delinsAC	GRCh37
NC_000010.9:g.89643767_89643768delinsAC	NCBI36
NG_007466.2:g.35592_35593delinsAC , LRG_311:g.35592_35593delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.85_86delinsAC	ENSP00000514759.2:p.Tyr29Thr
ENST00000710265.1:c.85_86delinsAC	ENSP00000518161.1:p.Tyr29Thr
ENST00000472832.3:c.85_86delinsAC	ENSP00000483066.2:p.Tyr29Thr
ENST00000688158.2:n.899+13592_899+13593delinsAC
ENST00000688922.2:c.85_86delinsAC	ENSP00000508742.2:p.Tyr29Thr
ENST00000700021.1:c.85_86delinsAC	ENSP00000514757.1:p.Tyr29Thr
ENST00000700022.1:c.85_86delinsAC	ENSP00000514758.1:p.Tyr29Thr
ENST00000706954.1:c.85_86delinsAC	ENSP00000516674.1:p.Tyr29Thr
ENST00000706955.1:c.*120_*121delinsAC	ENSP00000516675.1:n.*120_*121delinsAC
ENST00000686459.1:c.85_86delinsAC	ENSP00000508909.1:p.Tyr29Thr
ENST00000688158.1:c.*275+13592_*275+13593delinsAC	ENSP00000509254.1:n.*275+13592_*275+13593delinsAC
ENST00000688308.1:c.85_86delinsAC	ENSP00000508752.1:p.Tyr29Thr
ENST00000693560.1:c.604_605delinsAC	ENSP00000509861.1:p.Tyr202Thr
ENST00000371953.8:c.85_86delinsAC MANE Select	ENSP00000361021.3:p.Tyr29Thr
ENST00000371953.7:c.85_86delinsAC	ENSP00000361021.3:p.Tyr29Thr
ENST00000462694.1:n.87_88delinsAC
ENST00000610634.1:c.-18_-17delinsAC	ENSP00000477517.1:n.-18_-17delinsAC
NM_000314.5:c.85_86delinsAC	NP_000305.3:p.Tyr29Thr
NM_000314.6:c.85_86delinsAC	NP_000305.3:p.Tyr29Thr
NM_001304717.2:c.604_605delinsAC	NP_001291646.2:p.Tyr202Thr
NM_001304718.1:c.-621_-620delinsAC	NP_001291647.1:n.-621_-620delinsAC
XM_006717926.2:c.85_86delinsAC	XP_006717989.1:p.Tyr29Thr
XM_011539981.1:c.85_86delinsAC	XP_011538283.1:p.Tyr29Thr
XM_011539982.1:c.68+13592_68+13593delinsAC	XP_011538284.1:n.68+13592_68+13593delinsAC
XR_945789.1:n.797_798delinsAC
XR_945790.1:n.797_798delinsAC
XR_945791.1:n.797_798delinsAC
NM_000314.7:c.85_86delinsAC	NP_000305.3:p.Tyr29Thr
NM_001304717.5:c.604_605delinsAC	NP_001291646.4:p.Tyr202Thr
NM_001304718.2:c.-621_-620delinsAC	NP_001291647.1:n.-621_-620delinsAC
NM_000314.8:c.85_86delinsAC MANE Select	NP_000305.3:p.Tyr29Thr