Canonical Allele Identifier: CA891834990

Gene: PTEN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.87894066_87894068delinsTAT , CM000672.2:g.87894066_87894068delinsTAT	GRCh38
NC_000010.10:g.89653823_89653825delinsTAT , CM000672.1:g.89653823_89653825delinsTAT	GRCh37
NC_000010.9:g.89643803_89643805delinsTAT	NCBI36
NG_007466.2:g.35628_35630delinsTAT , LRG_311:g.35628_35630delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700029.2:c.121_123delinsTAT	ENSP00000514759.2:p.Arg41Tyr
ENST00000710265.1:c.121_123delinsTAT	ENSP00000518161.1:p.Arg41Tyr
ENST00000472832.3:c.121_123delinsTAT	ENSP00000483066.2:p.Arg41Tyr
ENST00000688158.2:n.899+13628_899+13630delinsTAT
ENST00000688922.2:c.121_123delinsTAT	ENSP00000508742.2:p.Arg41Tyr
ENST00000700021.1:c.121_123delinsTAT	ENSP00000514757.1:p.Arg41Tyr
ENST00000700022.1:c.121_123delinsTAT	ENSP00000514758.1:p.Arg41Tyr
ENST00000706954.1:c.121_123delinsTAT	ENSP00000516674.1:p.Arg41Tyr
ENST00000706955.1:c.*156_*158delinsTAT	ENSP00000516675.1:n.*156_*158delinsTAT
ENST00000686459.1:c.121_123delinsTAT	ENSP00000508909.1:p.Arg41Tyr
ENST00000688158.1:c.*275+13628_*275+13630delinsTAT	ENSP00000509254.1:n.*275+13628_*275+13630delinsTAT
ENST00000688308.1:c.121_123delinsTAT	ENSP00000508752.1:p.Arg41Tyr
ENST00000693560.1:c.640_642delinsTAT	ENSP00000509861.1:p.Arg214Tyr
ENST00000371953.8:c.121_123delinsTAT MANE Select	ENSP00000361021.3:p.Arg41Tyr
ENST00000371953.7:c.121_123delinsTAT	ENSP00000361021.3:p.Arg41Tyr
ENST00000462694.1:n.123_125delinsTAT
ENST00000610634.1:c.19_21delinsTAT	ENSP00000477517.1:p.Arg7Tyr
NM_000314.5:c.121_123delinsTAT	NP_000305.3:p.Arg41Tyr
NM_000314.6:c.121_123delinsTAT	NP_000305.3:p.Arg41Tyr
NM_001304717.2:c.640_642delinsTAT	NP_001291646.2:p.Arg214Tyr
NM_001304718.1:c.-585_-583delinsTAT	NP_001291647.1:n.-585_-583delinsTAT
XM_006717926.2:c.121_123delinsTAT	XP_006717989.1:p.Arg41Tyr
XM_011539981.1:c.121_123delinsTAT	XP_011538283.1:p.Arg41Tyr
XM_011539982.1:c.68+13628_68+13630delinsTAT	XP_011538284.1:n.68+13628_68+13630delinsTAT
XR_945789.1:n.833_835delinsTAT
XR_945790.1:n.833_835delinsTAT
XR_945791.1:n.833_835delinsTAT
NM_000314.7:c.121_123delinsTAT	NP_000305.3:p.Arg41Tyr
NM_001304717.5:c.640_642delinsTAT	NP_001291646.4:p.Arg214Tyr
NM_001304718.2:c.-585_-583delinsTAT	NP_001291647.1:n.-585_-583delinsTAT
NM_000314.8:c.121_123delinsTAT MANE Select	NP_000305.3:p.Arg41Tyr