Canonical Allele Identifier: CA891836764

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961068_87961070delinsACT , CM000672.2:g.87961068_87961070delinsACT	GRCh38
NC_000010.10:g.89720825_89720827delinsACT , CM000672.1:g.89720825_89720827delinsACT	GRCh37
NC_000010.9:g.89710805_89710807delinsACT	NCBI36
NG_007466.2:g.102630_102632delinsACT , LRG_311:g.102630_102632delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.1069_1071delinsACT	ENSP00000514759.2:p.Asp357Thr
ENST00000710265.1:c.976_978delinsACT	ENSP00000518161.1:p.Asp326Thr
ENST00000472832.3:c.976_978delinsACT	ENSP00000483066.2:p.Asp326Thr
ENST00000688158.2:n.1711_1713delinsACT
ENST00000688922.2:c.*806_*808delinsACT	ENSP00000508742.2:n.*806_*808delinsACT
ENST00000700021.1:c.931_933delinsACT	ENSP00000514757.1:p.Asp311Thr
ENST00000700022.1:c.*315_*317delinsACT	ENSP00000514758.1:n.*315_*317delinsACT
ENST00000700023.1:n.2134_2136delinsACT
ENST00000700024.1:n.2368_2370delinsACT
ENST00000700025.1:n.1745_1747delinsACT
ENST00000700026.1:n.613_615delinsACT
ENST00000706954.1:c.976_978delinsACT	ENSP00000516674.1:p.Asp326Thr
ENST00000706955.1:c.*1011_*1013delinsACT	ENSP00000516675.1:n.*1011_*1013delinsACT
ENST00000686459.1:c.*562_*564delinsACT	ENSP00000508909.1:n.*562_*564delinsACT
ENST00000688158.1:c.*1087_*1089delinsACT	ENSP00000509254.1:n.*1087_*1089delinsACT
ENST00000688308.1:c.976_978delinsACT	ENSP00000508752.1:p.Asp326Thr
ENST00000688922.1:c.897_899delinsACT
ENST00000693560.1:c.1495_1497delinsACT	ENSP00000509861.1:p.Asp499Thr
ENST00000371953.8:c.976_978delinsACT MANE Select	ENSP00000361021.3:p.Asp326Thr
ENST00000371953.7:c.976_978delinsACT	ENSP00000361021.3:p.Asp326Thr
ENST00000472832.2:c.403_405delinsACT	ENSP00000483066.1:p.Asp135Thr
NM_000314.5:c.976_978delinsACT	NP_000305.3:p.Asp326Thr
NM_000314.6:c.976_978delinsACT	NP_000305.3:p.Asp326Thr
NM_001304717.2:c.1495_1497delinsACT	NP_001291646.2:p.Asp499Thr
NM_001304718.1:c.385_387delinsACT	NP_001291647.1:p.Asp129Thr
XM_006717926.2:c.931_933delinsACT	XP_006717989.1:p.Asp311Thr
XM_011539981.1:c.976_978delinsACT	XP_011538283.1:p.Asp326Thr
XM_011539982.1:c.880_882delinsACT	XP_011538284.1:p.Asp294Thr
XR_945791.1:n.1546_1548delinsACT
NM_000314.7:c.976_978delinsACT	NP_000305.3:p.Asp326Thr
NM_001304717.5:c.1495_1497delinsACT	NP_001291646.4:p.Asp499Thr
NM_001304718.2:c.385_387delinsACT	NP_001291647.1:p.Asp129Thr
NM_000314.8:c.976_978delinsACT MANE Select	NP_000305.3:p.Asp326Thr