Canonical Allele Identifier: CA891835696

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960990_87960992delinsGAA , CM000672.2:g.87960990_87960992delinsGAA	GRCh38
NC_000010.10:g.89720747_89720749delinsGAA , CM000672.1:g.89720747_89720749delinsGAA	GRCh37
NC_000010.9:g.89710727_89710729delinsGAA	NCBI36
NG_007466.2:g.102552_102554delinsGAA , LRG_311:g.102552_102554delinsGAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.991_993delinsGAA	ENSP00000514759.2:p.Ile331Glu
ENST00000710265.1:c.898_900delinsGAA	ENSP00000518161.1:p.Ile300Glu
ENST00000472832.3:c.898_900delinsGAA	ENSP00000483066.2:p.Ile300Glu
ENST00000688158.2:n.1633_1635delinsGAA
ENST00000688922.2:c.*728_*730delinsGAA	ENSP00000508742.2:n.*728_*730delinsGAA
ENST00000700021.1:c.853_855delinsGAA	ENSP00000514757.1:p.Ile285Glu
ENST00000700022.1:c.*237_*239delinsGAA	ENSP00000514758.1:n.*237_*239delinsGAA
ENST00000700023.1:n.2056_2058delinsGAA
ENST00000700024.1:n.2290_2292delinsGAA
ENST00000700025.1:n.1667_1669delinsGAA
ENST00000700026.1:n.535_537delinsGAA
ENST00000706954.1:c.898_900delinsGAA	ENSP00000516674.1:p.Ile300Glu
ENST00000706955.1:c.*933_*935delinsGAA	ENSP00000516675.1:n.*933_*935delinsGAA
ENST00000686459.1:c.*484_*486delinsGAA	ENSP00000508909.1:n.*484_*486delinsGAA
ENST00000688158.1:c.*1009_*1011delinsGAA	ENSP00000509254.1:n.*1009_*1011delinsGAA
ENST00000688308.1:c.898_900delinsGAA	ENSP00000508752.1:p.Ile300Glu
ENST00000688922.1:c.819_821delinsGAA
ENST00000693560.1:c.1417_1419delinsGAA	ENSP00000509861.1:p.Ile473Glu
ENST00000371953.8:c.898_900delinsGAA MANE Select	ENSP00000361021.3:p.Ile300Glu
ENST00000371953.7:c.898_900delinsGAA	ENSP00000361021.3:p.Ile300Glu
ENST00000472832.2:c.325_327delinsGAA	ENSP00000483066.1:p.Ile109Glu
NM_000314.5:c.898_900delinsGAA	NP_000305.3:p.Ile300Glu
NM_000314.6:c.898_900delinsGAA	NP_000305.3:p.Ile300Glu
NM_001304717.2:c.1417_1419delinsGAA	NP_001291646.2:p.Ile473Glu
NM_001304718.1:c.307_309delinsGAA	NP_001291647.1:p.Ile103Glu
XM_006717926.2:c.853_855delinsGAA	XP_006717989.1:p.Ile285Glu
XM_011539981.1:c.898_900delinsGAA	XP_011538283.1:p.Ile300Glu
XM_011539982.1:c.802_804delinsGAA	XP_011538284.1:p.Ile268Glu
XR_945791.1:n.1468_1470delinsGAA
NM_000314.7:c.898_900delinsGAA	NP_000305.3:p.Ile300Glu
NM_001304717.5:c.1417_1419delinsGAA	NP_001291646.4:p.Ile473Glu
NM_001304718.2:c.307_309delinsGAA	NP_001291647.1:p.Ile103Glu
NM_000314.8:c.898_900delinsGAA MANE Select	NP_000305.3:p.Ile300Glu