Canonical Allele Identifier: CA891837963

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87933168_87933170delinsACT , CM000672.2:g.87933168_87933170delinsACT	GRCh38
NC_000010.10:g.89692925_89692927delinsACT , CM000672.1:g.89692925_89692927delinsACT	GRCh37
NC_000010.9:g.89682905_89682907delinsACT	NCBI36
NG_007466.2:g.74730_74732delinsACT , LRG_311:g.74730_74732delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.409_411delinsACT	ENSP00000514759.2:p.Ala137Thr
ENST00000710265.1:c.409_411delinsACT	ENSP00000518161.1:p.Ala137Thr
ENST00000472832.3:c.409_411delinsACT	ENSP00000483066.2:p.Ala137Thr
ENST00000688158.2:n.1144_1146delinsACT
ENST00000688922.2:c.*239_*241delinsACT	ENSP00000508742.2:n.*239_*241delinsACT
ENST00000700021.1:c.364_366delinsACT	ENSP00000514757.1:p.Ala122Thr
ENST00000700022.1:c.409_411delinsACT	ENSP00000514758.1:p.Ala137Thr
ENST00000700029.1:c.243_245delinsACT
ENST00000706954.1:c.409_411delinsACT	ENSP00000516674.1:p.Ala137Thr
ENST00000706955.1:c.*444_*446delinsACT	ENSP00000516675.1:n.*444_*446delinsACT
ENST00000686459.1:c.409_411delinsACT	ENSP00000508909.1:p.Ala137Thr
ENST00000688158.1:c.*520_*522delinsACT	ENSP00000509254.1:n.*520_*522delinsACT
ENST00000688308.1:c.409_411delinsACT	ENSP00000508752.1:p.Ala137Thr
ENST00000688922.1:c.330_332delinsACT
ENST00000693560.1:c.928_930delinsACT	ENSP00000509861.1:p.Ala310Thr
ENST00000371953.8:c.409_411delinsACT MANE Select	ENSP00000361021.3:p.Ala137Thr
ENST00000371953.7:c.409_411delinsACT	ENSP00000361021.3:p.Ala137Thr
ENST00000498703.1:n.235_237delinsACT
ENST00000610634.1:c.307_309delinsACT	ENSP00000477517.1:p.Ala103Thr
NM_000314.5:c.409_411delinsACT	NP_000305.3:p.Ala137Thr
NM_000314.6:c.409_411delinsACT	NP_000305.3:p.Ala137Thr
NM_001304717.2:c.928_930delinsACT	NP_001291646.2:p.Ala310Thr
NM_001304718.1:c.-342_-340delinsACT	NP_001291647.1:n.-342_-340delinsACT
XM_006717926.2:c.364_366delinsACT	XP_006717989.1:p.Ala122Thr
XM_011539981.1:c.409_411delinsACT	XP_011538283.1:p.Ala137Thr
XM_011539982.1:c.313_315delinsACT	XP_011538284.1:p.Ala105Thr
XR_945789.1:n.1121_1123delinsACT
XR_945790.1:n.1121_1123delinsACT
XR_945791.1:n.1121_1123delinsACT
NM_000314.7:c.409_411delinsACT	NP_000305.3:p.Ala137Thr
NM_001304717.5:c.928_930delinsACT	NP_001291646.4:p.Ala310Thr
NM_001304718.2:c.-342_-340delinsACT	NP_001291647.1:n.-342_-340delinsACT
NM_000314.8:c.409_411delinsACT MANE Select	NP_000305.3:p.Ala137Thr