Canonical Allele Identifier: CA891835029

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87960948_87960950delinsCAA , CM000672.2:g.87960948_87960950delinsCAA	GRCh38
NC_000010.10:g.89720705_89720707delinsCAA , CM000672.1:g.89720705_89720707delinsCAA	GRCh37
NC_000010.9:g.89710685_89710687delinsCAA	NCBI36
NG_007466.2:g.102510_102512delinsCAA , LRG_311:g.102510_102512delinsCAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.949_951delinsCAA	ENSP00000514759.2:p.Thr317Gln
ENST00000710265.1:c.856_858delinsCAA	ENSP00000518161.1:p.Thr286Gln
ENST00000472832.3:c.856_858delinsCAA	ENSP00000483066.2:p.Thr286Gln
ENST00000688158.2:n.1591_1593delinsCAA
ENST00000688922.2:c.*686_*688delinsCAA	ENSP00000508742.2:n.*686_*688delinsCAA
ENST00000700021.1:c.811_813delinsCAA	ENSP00000514757.1:p.Thr271Gln
ENST00000700022.1:c.*195_*197delinsCAA	ENSP00000514758.1:n.*195_*197delinsCAA
ENST00000700023.1:n.2014_2016delinsCAA
ENST00000700024.1:n.2248_2250delinsCAA
ENST00000700025.1:n.1625_1627delinsCAA
ENST00000700026.1:n.493_495delinsCAA
ENST00000700029.1:c.783_785delinsCAA
ENST00000706954.1:c.856_858delinsCAA	ENSP00000516674.1:p.Thr286Gln
ENST00000706955.1:c.*891_*893delinsCAA	ENSP00000516675.1:n.*891_*893delinsCAA
ENST00000686459.1:c.*442_*444delinsCAA	ENSP00000508909.1:n.*442_*444delinsCAA
ENST00000688158.1:c.*967_*969delinsCAA	ENSP00000509254.1:n.*967_*969delinsCAA
ENST00000688308.1:c.856_858delinsCAA	ENSP00000508752.1:p.Thr286Gln
ENST00000688922.1:c.777_779delinsCAA
ENST00000693560.1:c.1375_1377delinsCAA	ENSP00000509861.1:p.Thr459Gln
ENST00000371953.8:c.856_858delinsCAA MANE Select	ENSP00000361021.3:p.Thr286Gln
ENST00000371953.7:c.856_858delinsCAA	ENSP00000361021.3:p.Thr286Gln
ENST00000472832.2:c.283_285delinsCAA	ENSP00000483066.1:p.Thr95Gln
NM_000314.5:c.856_858delinsCAA	NP_000305.3:p.Thr286Gln
NM_000314.6:c.856_858delinsCAA	NP_000305.3:p.Thr286Gln
NM_001304717.2:c.1375_1377delinsCAA	NP_001291646.2:p.Thr459Gln
NM_001304718.1:c.265_267delinsCAA	NP_001291647.1:p.Thr89Gln
XM_006717926.2:c.811_813delinsCAA	XP_006717989.1:p.Thr271Gln
XM_011539981.1:c.856_858delinsCAA	XP_011538283.1:p.Thr286Gln
XM_011539982.1:c.760_762delinsCAA	XP_011538284.1:p.Thr254Gln
XR_945791.1:n.1426_1428delinsCAA
NM_000314.7:c.856_858delinsCAA	NP_000305.3:p.Thr286Gln
NM_001304717.5:c.1375_1377delinsCAA	NP_001291646.4:p.Thr459Gln
NM_001304718.2:c.265_267delinsCAA	NP_001291647.1:p.Thr89Gln
NM_000314.8:c.856_858delinsCAA MANE Select	NP_000305.3:p.Thr286Gln