Canonical Allele Identifier: CA891834803

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960933_87960935delinsGTT , CM000672.2:g.87960933_87960935delinsGTT	GRCh38
NC_000010.10:g.89720690_89720692delinsGTT , CM000672.1:g.89720690_89720692delinsGTT	GRCh37
NC_000010.9:g.89710670_89710672delinsGTT	NCBI36
NG_007466.2:g.102495_102497delinsGTT , LRG_311:g.102495_102497delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.934_936delinsGTT	ENSP00000514759.2:p.Pro312Val
ENST00000710265.1:c.841_843delinsGTT	ENSP00000518161.1:p.Pro281Val
ENST00000472832.3:c.841_843delinsGTT	ENSP00000483066.2:p.Pro281Val
ENST00000688158.2:n.1576_1578delinsGTT
ENST00000688922.2:c.*671_*673delinsGTT	ENSP00000508742.2:n.*671_*673delinsGTT
ENST00000700021.1:c.796_798delinsGTT	ENSP00000514757.1:p.Pro266Val
ENST00000700022.1:c.*180_*182delinsGTT	ENSP00000514758.1:n.*180_*182delinsGTT
ENST00000700023.1:n.1999_2001delinsGTT
ENST00000700024.1:n.2233_2235delinsGTT
ENST00000700025.1:n.1610_1612delinsGTT
ENST00000700026.1:n.478_480delinsGTT
ENST00000700029.1:c.768_770delinsGTT
ENST00000706954.1:c.841_843delinsGTT	ENSP00000516674.1:p.Pro281Val
ENST00000706955.1:c.*876_*878delinsGTT	ENSP00000516675.1:n.*876_*878delinsGTT
ENST00000686459.1:c.*427_*429delinsGTT	ENSP00000508909.1:n.*427_*429delinsGTT
ENST00000688158.1:c.*952_*954delinsGTT	ENSP00000509254.1:n.*952_*954delinsGTT
ENST00000688308.1:c.841_843delinsGTT	ENSP00000508752.1:p.Pro281Val
ENST00000688922.1:c.762_764delinsGTT
ENST00000693560.1:c.1360_1362delinsGTT	ENSP00000509861.1:p.Pro454Val
ENST00000371953.8:c.841_843delinsGTT MANE Select	ENSP00000361021.3:p.Pro281Val
ENST00000371953.7:c.841_843delinsGTT	ENSP00000361021.3:p.Pro281Val
ENST00000472832.2:c.268_270delinsGTT	ENSP00000483066.1:p.Pro90Val
NM_000314.5:c.841_843delinsGTT	NP_000305.3:p.Pro281Val
NM_000314.6:c.841_843delinsGTT	NP_000305.3:p.Pro281Val
NM_001304717.2:c.1360_1362delinsGTT	NP_001291646.2:p.Pro454Val
NM_001304718.1:c.250_252delinsGTT	NP_001291647.1:p.Pro84Val
XM_006717926.2:c.796_798delinsGTT	XP_006717989.1:p.Pro266Val
XM_011539981.1:c.841_843delinsGTT	XP_011538283.1:p.Pro281Val
XM_011539982.1:c.745_747delinsGTT	XP_011538284.1:p.Pro249Val
XR_945791.1:n.1411_1413delinsGTT
NM_000314.7:c.841_843delinsGTT	NP_000305.3:p.Pro281Val
NM_001304717.5:c.1360_1362delinsGTT	NP_001291646.4:p.Pro454Val
NM_001304718.2:c.250_252delinsGTT	NP_001291647.1:p.Pro84Val
NM_000314.8:c.841_843delinsGTT MANE Select	NP_000305.3:p.Pro281Val