Canonical Allele Identifier: CA891836921

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87961089_87961091delinsACT , CM000672.2:g.87961089_87961091delinsACT	GRCh38
NC_000010.10:g.89720846_89720848delinsACT , CM000672.1:g.89720846_89720848delinsACT	GRCh37
NC_000010.9:g.89710826_89710828delinsACT	NCBI36
NG_007466.2:g.102651_102653delinsACT , LRG_311:g.102651_102653delinsACT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.1090_1092delinsACT	ENSP00000514759.2:p.Ala364Thr
ENST00000710265.1:c.997_999delinsACT	ENSP00000518161.1:p.Ala333Thr
ENST00000472832.3:c.997_999delinsACT	ENSP00000483066.2:p.Ala333Thr
ENST00000688158.2:n.1732_1734delinsACT
ENST00000688922.2:c.*827_*829delinsACT	ENSP00000508742.2:n.*827_*829delinsACT
ENST00000700021.1:c.952_954delinsACT	ENSP00000514757.1:p.Ala318Thr
ENST00000700022.1:c.*336_*338delinsACT	ENSP00000514758.1:n.*336_*338delinsACT
ENST00000700023.1:n.2155_2157delinsACT
ENST00000700024.1:n.2389_2391delinsACT
ENST00000700025.1:n.1766_1768delinsACT
ENST00000700026.1:n.634_636delinsACT
ENST00000706954.1:c.997_999delinsACT	ENSP00000516674.1:p.Ala333Thr
ENST00000706955.1:c.*1032_*1034delinsACT	ENSP00000516675.1:n.*1032_*1034delinsACT
ENST00000686459.1:c.*583_*585delinsACT	ENSP00000508909.1:n.*583_*585delinsACT
ENST00000688158.1:c.*1108_*1110delinsACT	ENSP00000509254.1:n.*1108_*1110delinsACT
ENST00000688308.1:c.997_999delinsACT	ENSP00000508752.1:p.Ala333Thr
ENST00000688922.1:c.918_920delinsACT
ENST00000693560.1:c.1516_1518delinsACT	ENSP00000509861.1:p.Ala506Thr
ENST00000371953.8:c.997_999delinsACT MANE Select	ENSP00000361021.3:p.Ala333Thr
ENST00000371953.7:c.997_999delinsACT	ENSP00000361021.3:p.Ala333Thr
ENST00000472832.2:c.424_426delinsACT	ENSP00000483066.1:p.Ala142Thr
NM_000314.5:c.997_999delinsACT	NP_000305.3:p.Ala333Thr
NM_000314.6:c.997_999delinsACT	NP_000305.3:p.Ala333Thr
NM_001304717.2:c.1516_1518delinsACT	NP_001291646.2:p.Ala506Thr
NM_001304718.1:c.406_408delinsACT	NP_001291647.1:p.Ala136Thr
XM_006717926.2:c.952_954delinsACT	XP_006717989.1:p.Ala318Thr
XM_011539981.1:c.997_999delinsACT	XP_011538283.1:p.Ala333Thr
XM_011539982.1:c.901_903delinsACT	XP_011538284.1:p.Ala301Thr
XR_945791.1:n.1567_1569delinsACT
NM_000314.7:c.997_999delinsACT	NP_000305.3:p.Ala333Thr
NM_001304717.5:c.1516_1518delinsACT	NP_001291646.4:p.Ala506Thr
NM_001304718.2:c.406_408delinsACT	NP_001291647.1:p.Ala136Thr
NM_000314.8:c.997_999delinsACT MANE Select	NP_000305.3:p.Ala333Thr