Canonical Allele Identifier: CA891834771

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87925520_87925521delinsAT , CM000672.2:g.87925520_87925521delinsAT	GRCh38
NC_000010.10:g.89685277_89685278delinsAT , CM000672.1:g.89685277_89685278delinsAT	GRCh37
NC_000010.9:g.89675257_89675258delinsAT	NCBI36
NG_007466.2:g.67082_67083delinsAT , LRG_311:g.67082_67083delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.172_173delinsAT	ENSP00000514759.2:p.Asp58Ile
ENST00000710265.1:c.172_173delinsAT	ENSP00000518161.1:p.Asp58Ile
ENST00000472832.3:c.172_173delinsAT	ENSP00000483066.2:p.Asp58Ile
ENST00000688158.2:n.907_908delinsAT
ENST00000688922.2:c.172_173delinsAT	ENSP00000508742.2:p.Asp58Ile
ENST00000700021.1:c.165-5526_165-5525delinsAT	ENSP00000514757.1:n.165-5526_165-5525delinsAT
ENST00000700022.1:c.172_173delinsAT	ENSP00000514758.1:p.Asp58Ile
ENST00000700029.1:c.6_7delinsAT
ENST00000706954.1:c.172_173delinsAT	ENSP00000516674.1:p.Asp58Ile
ENST00000706955.1:c.*207_*208delinsAT	ENSP00000516675.1:n.*207_*208delinsAT
ENST00000686459.1:c.172_173delinsAT	ENSP00000508909.1:p.Asp58Ile
ENST00000688158.1:c.*283_*284delinsAT	ENSP00000509254.1:n.*283_*284delinsAT
ENST00000688308.1:c.172_173delinsAT	ENSP00000508752.1:p.Asp58Ile
ENST00000688922.1:c.41_42delinsAT
ENST00000693560.1:c.691_692delinsAT	ENSP00000509861.1:p.Asp231Ile
ENST00000371953.8:c.172_173delinsAT MANE Select	ENSP00000361021.3:p.Asp58Ile
ENST00000371953.7:c.172_173delinsAT	ENSP00000361021.3:p.Asp58Ile
ENST00000610634.1:c.70_71delinsAT	ENSP00000477517.1:p.Asp24Ile
NM_000314.5:c.172_173delinsAT	NP_000305.3:p.Asp58Ile
NM_000314.6:c.172_173delinsAT	NP_000305.3:p.Asp58Ile
NM_001304717.2:c.691_692delinsAT	NP_001291646.2:p.Asp231Ile
NM_001304718.1:c.-541-5526_-541-5525delinsAT	NP_001291647.1:n.-541-5526_-541-5525delinsAT
XM_006717926.2:c.165-5526_165-5525delinsAT	XP_006717989.1:n.165-5526_165-5525delinsAT
XM_011539981.1:c.172_173delinsAT	XP_011538283.1:p.Asp58Ile
XM_011539982.1:c.76_77delinsAT	XP_011538284.1:p.Asp26Ile
XR_945789.1:n.884_885delinsAT
XR_945790.1:n.884_885delinsAT
XR_945791.1:n.884_885delinsAT
NM_000314.7:c.172_173delinsAT	NP_000305.3:p.Asp58Ile
NM_001304717.5:c.691_692delinsAT	NP_001291646.4:p.Asp231Ile
NM_001304718.2:c.-541-5526_-541-5525delinsAT	NP_001291647.1:n.-541-5526_-541-5525delinsAT
NM_000314.8:c.172_173delinsAT MANE Select	NP_000305.3:p.Asp58Ile