Canonical Allele Identifier: CA891835721

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960990_87960992delinsGCT , CM000672.2:g.87960990_87960992delinsGCT	GRCh38
NC_000010.10:g.89720747_89720749delinsGCT , CM000672.1:g.89720747_89720749delinsGCT	GRCh37
NC_000010.9:g.89710727_89710729delinsGCT	NCBI36
NG_007466.2:g.102552_102554delinsGCT , LRG_311:g.102552_102554delinsGCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.991_993delinsGCT	ENSP00000514759.2:p.Ile331Ala
ENST00000710265.1:c.898_900delinsGCT	ENSP00000518161.1:p.Ile300Ala
ENST00000472832.3:c.898_900delinsGCT	ENSP00000483066.2:p.Ile300Ala
ENST00000688158.2:n.1633_1635delinsGCT
ENST00000688922.2:c.*728_*730delinsGCT	ENSP00000508742.2:n.*728_*730delinsGCT
ENST00000700021.1:c.853_855delinsGCT	ENSP00000514757.1:p.Ile285Ala
ENST00000700022.1:c.*237_*239delinsGCT	ENSP00000514758.1:n.*237_*239delinsGCT
ENST00000700023.1:n.2056_2058delinsGCT
ENST00000700024.1:n.2290_2292delinsGCT
ENST00000700025.1:n.1667_1669delinsGCT
ENST00000700026.1:n.535_537delinsGCT
ENST00000706954.1:c.898_900delinsGCT	ENSP00000516674.1:p.Ile300Ala
ENST00000706955.1:c.*933_*935delinsGCT	ENSP00000516675.1:n.*933_*935delinsGCT
ENST00000686459.1:c.*484_*486delinsGCT	ENSP00000508909.1:n.*484_*486delinsGCT
ENST00000688158.1:c.*1009_*1011delinsGCT	ENSP00000509254.1:n.*1009_*1011delinsGCT
ENST00000688308.1:c.898_900delinsGCT	ENSP00000508752.1:p.Ile300Ala
ENST00000688922.1:c.819_821delinsGCT
ENST00000693560.1:c.1417_1419delinsGCT	ENSP00000509861.1:p.Ile473Ala
ENST00000371953.8:c.898_900delinsGCT MANE Select	ENSP00000361021.3:p.Ile300Ala
ENST00000371953.7:c.898_900delinsGCT	ENSP00000361021.3:p.Ile300Ala
ENST00000472832.2:c.325_327delinsGCT	ENSP00000483066.1:p.Ile109Ala
NM_000314.5:c.898_900delinsGCT	NP_000305.3:p.Ile300Ala
NM_000314.6:c.898_900delinsGCT	NP_000305.3:p.Ile300Ala
NM_001304717.2:c.1417_1419delinsGCT	NP_001291646.2:p.Ile473Ala
NM_001304718.1:c.307_309delinsGCT	NP_001291647.1:p.Ile103Ala
XM_006717926.2:c.853_855delinsGCT	XP_006717989.1:p.Ile285Ala
XM_011539981.1:c.898_900delinsGCT	XP_011538283.1:p.Ile300Ala
XM_011539982.1:c.802_804delinsGCT	XP_011538284.1:p.Ile268Ala
XR_945791.1:n.1468_1470delinsGCT
NM_000314.7:c.898_900delinsGCT	NP_000305.3:p.Ile300Ala
NM_001304717.5:c.1417_1419delinsGCT	NP_001291646.4:p.Ile473Ala
NM_001304718.2:c.307_309delinsGCT	NP_001291647.1:p.Ile103Ala
NM_000314.8:c.898_900delinsGCT MANE Select	NP_000305.3:p.Ile300Ala