Canonical Allele Identifier: CA891834782

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960933_87960935delinsGAT , CM000672.2:g.87960933_87960935delinsGAT	GRCh38
NC_000010.10:g.89720690_89720692delinsGAT , CM000672.1:g.89720690_89720692delinsGAT	GRCh37
NC_000010.9:g.89710670_89710672delinsGAT	NCBI36
NG_007466.2:g.102495_102497delinsGAT , LRG_311:g.102495_102497delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.934_936delinsGAT	ENSP00000514759.2:p.Pro312Asp
ENST00000710265.1:c.841_843delinsGAT	ENSP00000518161.1:p.Pro281Asp
ENST00000472832.3:c.841_843delinsGAT	ENSP00000483066.2:p.Pro281Asp
ENST00000688158.2:n.1576_1578delinsGAT
ENST00000688922.2:c.*671_*673delinsGAT	ENSP00000508742.2:n.*671_*673delinsGAT
ENST00000700021.1:c.796_798delinsGAT	ENSP00000514757.1:p.Pro266Asp
ENST00000700022.1:c.*180_*182delinsGAT	ENSP00000514758.1:n.*180_*182delinsGAT
ENST00000700023.1:n.1999_2001delinsGAT
ENST00000700024.1:n.2233_2235delinsGAT
ENST00000700025.1:n.1610_1612delinsGAT
ENST00000700026.1:n.478_480delinsGAT
ENST00000700029.1:c.768_770delinsGAT
ENST00000706954.1:c.841_843delinsGAT	ENSP00000516674.1:p.Pro281Asp
ENST00000706955.1:c.*876_*878delinsGAT	ENSP00000516675.1:n.*876_*878delinsGAT
ENST00000686459.1:c.*427_*429delinsGAT	ENSP00000508909.1:n.*427_*429delinsGAT
ENST00000688158.1:c.*952_*954delinsGAT	ENSP00000509254.1:n.*952_*954delinsGAT
ENST00000688308.1:c.841_843delinsGAT	ENSP00000508752.1:p.Pro281Asp
ENST00000688922.1:c.762_764delinsGAT
ENST00000693560.1:c.1360_1362delinsGAT	ENSP00000509861.1:p.Pro454Asp
ENST00000371953.8:c.841_843delinsGAT MANE Select	ENSP00000361021.3:p.Pro281Asp
ENST00000371953.7:c.841_843delinsGAT	ENSP00000361021.3:p.Pro281Asp
ENST00000472832.2:c.268_270delinsGAT	ENSP00000483066.1:p.Pro90Asp
NM_000314.5:c.841_843delinsGAT	NP_000305.3:p.Pro281Asp
NM_000314.6:c.841_843delinsGAT	NP_000305.3:p.Pro281Asp
NM_001304717.2:c.1360_1362delinsGAT	NP_001291646.2:p.Pro454Asp
NM_001304718.1:c.250_252delinsGAT	NP_001291647.1:p.Pro84Asp
XM_006717926.2:c.796_798delinsGAT	XP_006717989.1:p.Pro266Asp
XM_011539981.1:c.841_843delinsGAT	XP_011538283.1:p.Pro281Asp
XM_011539982.1:c.745_747delinsGAT	XP_011538284.1:p.Pro249Asp
XR_945791.1:n.1411_1413delinsGAT
NM_000314.7:c.841_843delinsGAT	NP_000305.3:p.Pro281Asp
NM_001304717.5:c.1360_1362delinsGAT	NP_001291646.4:p.Pro454Asp
NM_001304718.2:c.250_252delinsGAT	NP_001291647.1:p.Pro84Asp
NM_000314.8:c.841_843delinsGAT MANE Select	NP_000305.3:p.Pro281Asp