Canonical Allele Identifier: CA891835154

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925547_87925549delinsGCT , CM000672.2:g.87925547_87925549delinsGCT	GRCh38
NC_000010.10:g.89685304_89685306delinsGCT , CM000672.1:g.89685304_89685306delinsGCT	GRCh37
NC_000010.9:g.89675284_89675286delinsGCT	NCBI36
NG_007466.2:g.67109_67111delinsGCT , LRG_311:g.67109_67111delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.199_201delinsGCT	ENSP00000514759.2:p.Ile67Ala
ENST00000710265.1:c.199_201delinsGCT	ENSP00000518161.1:p.Ile67Ala
ENST00000472832.3:c.199_201delinsGCT	ENSP00000483066.2:p.Ile67Ala
ENST00000688158.2:n.934_936delinsGCT
ENST00000688922.2:c.199_201delinsGCT	ENSP00000508742.2:p.Ile67Ala
ENST00000700021.1:c.165-5499_165-5497delinsGCT	ENSP00000514757.1:n.165-5499_165-5497delinsGCT
ENST00000700022.1:c.199_201delinsGCT	ENSP00000514758.1:p.Ile67Ala
ENST00000700029.1:c.33_35delinsGCT
ENST00000706954.1:c.199_201delinsGCT	ENSP00000516674.1:p.Ile67Ala
ENST00000706955.1:c.*234_*236delinsGCT	ENSP00000516675.1:n.*234_*236delinsGCT
ENST00000686459.1:c.199_201delinsGCT	ENSP00000508909.1:p.Ile67Ala
ENST00000688158.1:c.*310_*312delinsGCT	ENSP00000509254.1:n.*310_*312delinsGCT
ENST00000688308.1:c.199_201delinsGCT	ENSP00000508752.1:p.Ile67Ala
ENST00000688922.1:c.68_70delinsGCT
ENST00000693560.1:c.718_720delinsGCT	ENSP00000509861.1:p.Ile240Ala
ENST00000371953.8:c.199_201delinsGCT MANE Select	ENSP00000361021.3:p.Ile67Ala
ENST00000371953.7:c.199_201delinsGCT	ENSP00000361021.3:p.Ile67Ala
ENST00000498703.1:n.25_27delinsGCT
ENST00000610634.1:c.97_99delinsGCT	ENSP00000477517.1:p.Ile33Ala
NM_000314.5:c.199_201delinsGCT	NP_000305.3:p.Ile67Ala
NM_000314.6:c.199_201delinsGCT	NP_000305.3:p.Ile67Ala
NM_001304717.2:c.718_720delinsGCT	NP_001291646.2:p.Ile240Ala
NM_001304718.1:c.-541-5499_-541-5497delinsGCT	NP_001291647.1:n.-541-5499_-541-5497delinsGCT
XM_006717926.2:c.165-5499_165-5497delinsGCT	XP_006717989.1:n.165-5499_165-5497delinsGCT
XM_011539981.1:c.199_201delinsGCT	XP_011538283.1:p.Ile67Ala
XM_011539982.1:c.103_105delinsGCT	XP_011538284.1:p.Ile35Ala
XR_945789.1:n.911_913delinsGCT
XR_945790.1:n.911_913delinsGCT
XR_945791.1:n.911_913delinsGCT
NM_000314.7:c.199_201delinsGCT	NP_000305.3:p.Ile67Ala
NM_001304717.5:c.718_720delinsGCT	NP_001291646.4:p.Ile240Ala
NM_001304718.2:c.-541-5499_-541-5497delinsGCT	NP_001291647.1:n.-541-5499_-541-5497delinsGCT
NM_000314.8:c.199_201delinsGCT MANE Select	NP_000305.3:p.Ile67Ala