Canonical Allele Identifier: CA891840394

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925532_87925533delinsGT , CM000672.2:g.87925532_87925533delinsGT	GRCh38
NC_000010.10:g.89685289_89685290delinsGT , CM000672.1:g.89685289_89685290delinsGT	GRCh37
NC_000010.9:g.89675269_89675270delinsGT	NCBI36
NG_007466.2:g.67094_67095delinsGT , LRG_311:g.67094_67095delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000700029.2:c.184_185delinsGT	ENSP00000514759.2:p.Lys62Val
ENST00000710265.1:c.184_185delinsGT	ENSP00000518161.1:p.Lys62Val
ENST00000472832.3:c.184_185delinsGT	ENSP00000483066.2:p.Lys62Val
ENST00000688158.2:n.919_920delinsGT
ENST00000688922.2:c.184_185delinsGT	ENSP00000508742.2:p.Lys62Val
ENST00000700021.1:c.165-5514_165-5513delinsGT	ENSP00000514757.1:n.165-5514_165-5513deli...
ENST00000700022.1:c.184_185delinsGT	ENSP00000514758.1:p.Lys62Val
ENST00000700029.1:c.18_19delinsGT
ENST00000706954.1:c.184_185delinsGT	ENSP00000516674.1:p.Lys62Val
ENST00000706955.1:c.*219_*220delinsGT	ENSP00000516675.1:n.*219_*220delinsGT
ENST00000686459.1:c.184_185delinsGT	ENSP00000508909.1:p.Lys62Val
ENST00000688158.1:c.*295_*296delinsGT	ENSP00000509254.1:n.*295_*296delinsGT
ENST00000688308.1:c.184_185delinsGT	ENSP00000508752.1:p.Lys62Val
ENST00000688922.1:c.53_54delinsGT
ENST00000693560.1:c.703_704delinsGT	ENSP00000509861.1:p.Lys235Val
ENST00000371953.8:c.184_185delinsGT MANE Select	ENSP00000361021.3:p.Lys62Val
ENST00000371953.7:c.184_185delinsGT	ENSP00000361021.3:p.Lys62Val
ENST00000498703.1:n.10_11delinsGT
ENST00000610634.1:c.82_83delinsGT	ENSP00000477517.1:p.Lys28Val
NM_000314.5:c.184_185delinsGT	NP_000305.3:p.Lys62Val
NM_000314.6:c.184_185delinsGT	NP_000305.3:p.Lys62Val
NM_001304717.2:c.703_704delinsGT	NP_001291646.2:p.Lys235Val
NM_001304718.1:c.-541-5514_-541-5513delinsGT	NP_001291647.1:n.-541-5514_-541-5513delin...
XM_006717926.2:c.165-5514_165-5513delinsGT	XP_006717989.1:n.165-5514_165-5513delinsG...
XM_011539981.1:c.184_185delinsGT	XP_011538283.1:p.Lys62Val
XM_011539982.1:c.88_89delinsGT	XP_011538284.1:p.Lys30Val
XR_945789.1:n.896_897delinsGT
XR_945790.1:n.896_897delinsGT
XR_945791.1:n.896_897delinsGT
NM_000314.7:c.184_185delinsGT	NP_000305.3:p.Lys62Val
NM_001304717.5:c.703_704delinsGT	NP_001291646.4:p.Lys235Val
NM_001304718.2:c.-541-5514_-541-5513delinsGT	NP_001291647.1:n.-541-5514_-541-5513delin...
NM_000314.8:c.184_185delinsGT MANE Select	NP_000305.3:p.Lys62Val