Canonical Allele Identifier: CA891834970

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894066_87894068delinsCAT , CM000672.2:g.87894066_87894068delinsCAT	GRCh38
NC_000010.10:g.89653823_89653825delinsCAT , CM000672.1:g.89653823_89653825delinsCAT	GRCh37
NC_000010.9:g.89643803_89643805delinsCAT	NCBI36
NG_007466.2:g.35628_35630delinsCAT , LRG_311:g.35628_35630delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.121_123delinsCAT	ENSP00000514759.2:p.Arg41His
ENST00000710265.1:c.121_123delinsCAT	ENSP00000518161.1:p.Arg41His
ENST00000472832.3:c.121_123delinsCAT	ENSP00000483066.2:p.Arg41His
ENST00000688158.2:n.899+13628_899+13630delinsCAT
ENST00000688922.2:c.121_123delinsCAT	ENSP00000508742.2:p.Arg41His
ENST00000700021.1:c.121_123delinsCAT	ENSP00000514757.1:p.Arg41His
ENST00000700022.1:c.121_123delinsCAT	ENSP00000514758.1:p.Arg41His
ENST00000706954.1:c.121_123delinsCAT	ENSP00000516674.1:p.Arg41His
ENST00000706955.1:c.*156_*158delinsCAT	ENSP00000516675.1:n.*156_*158delinsCAT
ENST00000686459.1:c.121_123delinsCAT	ENSP00000508909.1:p.Arg41His
ENST00000688158.1:c.*275+13628_*275+13630delinsCAT	ENSP00000509254.1:n.*275+13628_*275+13630delinsCAT
ENST00000688308.1:c.121_123delinsCAT	ENSP00000508752.1:p.Arg41His
ENST00000693560.1:c.640_642delinsCAT	ENSP00000509861.1:p.Arg214His
ENST00000371953.8:c.121_123delinsCAT MANE Select	ENSP00000361021.3:p.Arg41His
ENST00000371953.7:c.121_123delinsCAT	ENSP00000361021.3:p.Arg41His
ENST00000462694.1:n.123_125delinsCAT
ENST00000610634.1:c.19_21delinsCAT	ENSP00000477517.1:p.Arg7His
NM_000314.5:c.121_123delinsCAT	NP_000305.3:p.Arg41His
NM_000314.6:c.121_123delinsCAT	NP_000305.3:p.Arg41His
NM_001304717.2:c.640_642delinsCAT	NP_001291646.2:p.Arg214His
NM_001304718.1:c.-585_-583delinsCAT	NP_001291647.1:n.-585_-583delinsCAT
XM_006717926.2:c.121_123delinsCAT	XP_006717989.1:p.Arg41His
XM_011539981.1:c.121_123delinsCAT	XP_011538283.1:p.Arg41His
XM_011539982.1:c.68+13628_68+13630delinsCAT	XP_011538284.1:n.68+13628_68+13630delinsCAT
XR_945789.1:n.833_835delinsCAT
XR_945790.1:n.833_835delinsCAT
XR_945791.1:n.833_835delinsCAT
NM_000314.7:c.121_123delinsCAT	NP_000305.3:p.Arg41His
NM_001304717.5:c.640_642delinsCAT	NP_001291646.4:p.Arg214His
NM_001304718.2:c.-585_-583delinsCAT	NP_001291647.1:n.-585_-583delinsCAT
NM_000314.8:c.121_123delinsCAT MANE Select	NP_000305.3:p.Arg41His